Canonical Allele Identifier: PA2829600793
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2129189
ClinVar RCV Id: RCV003040416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Cys51Arg
CA378924737
NM_005343.4:c.151T>C