Canonical Allele Identifier: PA2829601104
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 936794
ClinVar RCV Id: RCV001205671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala155Ser
CA378921217
NM_005343.4:c.463G>T