Canonical Allele Identifier: PA2580198924
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2014533
ClinVar RCV Id: RCV002861544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ser98del
CA2580083836
NM_001318054.2:c.292_294del