Canonical Allele Identifier: PA101489
Gene: HINT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37318
ClinVar RCV Id: RCV000030858 RCV002433480
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005331.1:p.Gly93Asp
CA130165
NM_005340.7:c.278G>A