Allele Registry

Canonical Allele Identifier: PA2825964741

Gene: PYGL HGNC NCBI

ClinVar RCV:

RCV000020503

RCV000594520

ClinVar Variation:

21338

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157412.1:p.Gln13Pro	CA341924 NM_001163940.2:c.38A>C