Canonical Allele Identifier: PA101459
Gene: HINT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37312
ClinVar RCV Id: RCV000030852 RCV000235535 RCV001814014 RCV002426529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005331.1:p.Arg37Pro
CA130158
NM_005340.7:c.110G>C