Allele Registry

Canonical Allele Identifier: PA2825964838

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV001930963

ClinVar Variation:

1418533

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Arg365Gly	CA389688500 NM_001163940.2:c.1093C>G