Allele Registry

Canonical Allele Identifier: PA2829180030

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV000477735

RCV001662450

RCV001777163

ClinVar Variation:

417743

HGVS (amino-acid)	Matching Registered Transcripts
NP_001375421.1:p.Thr1260Met	CA2824227 NM_001388492.1:c.3779C>T