Allele Registry

Canonical Allele Identifier: PA2825964901

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020500

ClinVar Variation:

21335

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Lys647Thr	CA341918 NM_001163940.2:c.1940A>C