Allele Registry

Canonical Allele Identifier: PA2825964900

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020498

ClinVar Variation:

21333

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Ser641Thr	CA341914 NM_001163940.2:c.1921T>A