Allele Registry

Canonical Allele Identifier: PA103568

Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12603

ClinVar RCV Id: RCV000013437 RCV000418547 RCV000422263 RCV000430806 RCV000417508 RCV000435619 RCV000423413 RCV000423622 RCV000207503 RCV000440663 RCV000425989 RCV000426130 RCV000428375 RCV000441501 RCV000444092 RCV000433266 RCV000445257 RCV000428172 RCV000433587 RCV000423741 RCV000425511 RCV000623953 RCV000432956 RCV000762848 RCV000435805 RCV000436832 RCV000442448 RCV000445090 RCV001813186 RCV001257536

ClinVar Variation Id: 40430

ClinVar RCV Id: RCV000157929

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Gly12Ala	CA256486 NM_001130442.3:c.35G>C CA296077 NM_001130442.3:c.35_36delinsCT