Canonical Allele Identifier: PA916022187
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 660554
ClinVar RCV Id: RCV000817769
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Gly99Arg
CA378921005
NM_001318054.2:c.295G>C