Canonical Allele Identifier: PA2825692511
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1720993
ClinVar RCV Id: RCV002300209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ser177Thr
CA378921012
NM_001130442.3:c.530G>C