Allele Registry

Canonical Allele Identifier: PA645485619

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV000477735

RCV001662450

RCV001777163

ClinVar Variation:

417743

HGVS (amino-acid)	Matching Registered Transcripts
NP_002102.4:p.Thr1262Met	CA2824227 NM_002111.8:c.3785C>T