Canonical Allele Identifier: PA2499247993
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1008068
ClinVar RCV Id: RCV001305343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Tyr78His
CA378921197
NM_001318054.2:c.232T>C