Canonical Allele Identifier: PA2580532839
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1993499
ClinVar RCV Id: RCV002801443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Asn85Asp
CA5779379
NM_176795.5:c.253A>G