Canonical Allele Identifier: PA2573242971
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1422549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro179Ser
CA378920992
NM_005343.4:c.535C>T