Canonical Allele Identifier: PA915994317
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 654278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly180Ser
CA5779210
NM_005343.4:c.538G>A