Canonical Allele Identifier: PA2829601178
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2014533
ClinVar RCV Id: RCV002861544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ser177del
CA2580083836
NM_005343.4:c.529_531del