Canonical Allele Identifier: PA2499247996
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1019189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.His87Arg
CA378921139
NM_001318054.2:c.260A>G