Allele Registry

Canonical Allele Identifier: PA645436764

Gene: AGL HGNC NCBI

ClinVar RCV:

RCV000335847

RCV001567373

RCV002519359

ClinVar Variation:

291333

HGVS (amino-acid)	Matching Registered Transcripts
NP_000633.2:p.His587Tyr	CA966587 NM_000642.3:c.1759C>T