Canonical Allele Identifier: PA2579932271
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1043469
ClinVar RCV Id: RCV001347584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr87Ile
CA378924419
NM_001130442.3:c.260C>T