Allele Registry

Canonical Allele Identifier: PA2825964936

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020501

ClinVar Variation:

21336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Tyr787His	CA341920 NM_001163940.2:c.2359T>C