Canonical Allele Identifier: PA101499
Gene: HINT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37315
ClinVar RCV Id: RCV000030855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005331.1:p.His112Asn
CA130161
NM_005340.7:c.334C>A