Canonical Allele Identifier: PA296062
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40439
ClinVar RCV Id: RCV000157920 RCV000143899 RCV000524082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile93Val
CA296061
NM_005343.4:c.277A>G