Allele Registry

Canonical Allele Identifier: PA2825964899

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020499

ClinVar Variation:

21334

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Ser641Leu	CA341916 NM_001163940.2:c.1922C>T