Allele Registry

Canonical Allele Identifier: PA2573219725

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV002151631

ClinVar Variation:

1651223

HGVS (amino-acid)	Matching Registered Transcripts
NP_002102.4:p.Ile1093Met	CA2824092 NM_002111.8:c.3279T>G