Canonical Allele Identifier: PA256487
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12603
ClinVar Variation Id: 40430
ClinVar RCV Id: RCV000157929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Ala
CA256486
NM_005343.4:c.35G>C
CA296077
NM_005343.4:c.35_36delinsCT