Canonical Allele Identifier: PA2579933414
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2178513
ClinVar RCV Id: RCV002595577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly77Asp
CA378924567
NM_001130442.3:c.230G>A