Canonical Allele Identifier: PA913197060
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 618166
ClinVar RCV Id: RCV000756250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Met72Leu
CA378924601
NM_005343.4:c.214A>T
CA378924603
NM_005343.4:c.214A>C