Allele Registry

Canonical Allele Identifier: PA2829180262

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV000477714

ClinVar Variation:

417745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001375421.1:p.Phe2717Tyr	CA16616860 NM_001388492.1:c.8150T>A