Canonical Allele Identifier: PA2579931288
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2093477
ClinVar RCV Id: RCV002996801
ClinVar Variation Id: 2156214
ClinVar RCV Id: RCV003084081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly151Arg
CA378921265
NM_001130442.3:c.451G>C
CA378921267
NM_001130442.3:c.451G>A