Canonical Allele Identifier: PA645475417
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240136
ClinVar RCV Id: RCV000228331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.His166Gln
CA10582922
NM_005343.4:c.498C>A
CA378921136
NM_005343.4:c.498C>G