Allele Registry

Canonical Allele Identifier: PA645485614

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV000477706

RCV001851126

ClinVar Variation:

417742

HGVS (amino-acid)	Matching Registered Transcripts
NP_002102.4:p.Pro705Leu	CA2823749 NM_002111.8:c.2114C>T