Canonical Allele Identifier: PA2579933406
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1993499
ClinVar RCV Id: RCV002801443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asn85Asp
CA5779379
NM_001130442.3:c.253A>G