Canonical Allele Identifier: PA891850525
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 579709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg164Trp
CA5779220
NM_005343.4:c.490C>T