Canonical Allele Identifier: PA2826977549
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 724759
ClinVar RCV Id: RCV000898724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro100Ala
CA378920995
NM_001318054.2:c.298C>G