Canonical Allele Identifier: PA2579931372
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 160364
ClinVar RCV Id: RCV000148033 RCV000157918 RCV000418550 RCV000437086 RCV000662268 RCV001813393 RCV001844808
ClinVar Variation Id: 376320
ClinVar RCV Id: RCV000435225
ClinVar Variation Id: 376321
ClinVar RCV Id: RCV000418005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gln61Arg
CA173968
NM_001130442.3:c.182A>G
CA16602766
NM_001130442.3:c.182_183delinsGT
CA16602767
NM_001130442.3:c.182_183delinsGA
CA645569138
NM_001130442.3:c.181_182delinsAG