Canonical Allele Identifier: PA2826977563
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1407404
ClinVar RCV Id: RCV001918427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Cys105Ser
CA378920918
NM_001318054.2:c.314G>C
CA378920926
NM_001318054.2:c.313T>A