Canonical Allele Identifier: PA2741859581
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 3015521
ClinVar RCV Id: RCV003871128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Thr79Lys
CA378921186
NM_001318054.2:c.236C>A