Canonical Allele Identifier: PA2829179853
Gene: HTT HGNC NCBI

Linked Data

ClinVar Variation Id: 2381651
ClinVar RCV Id: RCV002674527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001375421.1:p.Gln35Pro
CA248405
NM_001388492.1:c.104A>C