Canonical Allele Identifier: PA180999
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg169Trp
CA180998
NM_005343.4:c.505C>T