Canonical Allele Identifier: PA916022182
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Arg90Trp
CA180998
NM_001318054.2:c.268C>T