Canonical Allele Identifier: PA1139706689
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 946957
ClinVar RCV Id: RCV001217922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Met182Leu
CA378920954
NM_005343.4:c.544A>C
CA378920956
NM_005343.4:c.544A>T