Allele Registry

Canonical Allele Identifier: PA2825964888

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020495

ClinVar Variation:

21330

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Asn598Ile	CA341910 NM_001163940.2:c.1793A>T