Allele Registry

Canonical Allele Identifier: PA645485622

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV000477714

ClinVar Variation:

417745

HGVS (amino-acid)	Matching Registered Transcripts
NP_002102.4:p.Phe2719Tyr	CA16616860 NM_002111.8:c.8156T>A