Allele Registry

Canonical Allele Identifier: PA2825964795

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000592955

RCV000989223

ClinVar Variation:

499130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Gly199Ser	CA7183705 NM_001163940.2:c.595G>A