Canonical Allele Identifier: PA2579932541
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1062564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg68Gly
CA378924632
NM_001130442.3:c.202C>G