Allele Registry

Canonical Allele Identifier: PA2573219934

Gene: HTT HGNC NCBI

ClinVar RCV:

RCV002092237

ClinVar Variation:

1531045

HGVS (amino-acid)	Matching Registered Transcripts
NP_002102.4:p.Val2788Ile	CA2825672 NM_002111.8:c.8362G>A