Canonical Allele Identifier: PA645475331
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376318
ClinVar Variation Id: 376319
ClinVar RCV Id: RCV000428014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gln61His
CA16602764
NM_005343.4:c.183G>T
CA16602765
NM_005343.4:c.183G>C