Canonical Allele Identifier: PA916022176
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 517437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Arg82His
CA5779221
NM_001318054.2:c.245G>A