Canonical Allele Identifier: PA122556
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12612
ClinVar RCV Id: RCV000013446 RCV000149830 RCV000038460 RCV000029210 RCV000212496 RCV000429375 RCV001255681 RCV001375956 RCV001813189
ClinVar Variation Id: 180854
ClinVar RCV Id: RCV001678586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Asp
CA122555
NM_005343.4:c.35G>A
CA296072
NM_005343.4:c.35_36delinsAT