Canonical Allele Identifier: PA645482375
Gene: HINT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 246535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005331.1:p.Asp68Val
CA3398610
NM_005340.7:c.203A>T