Canonical Allele Identifier: PA2825964796
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 21339
ClinVar RCV Id: RCV000020504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Gly199Asp
CA341926
NM_001163940.2:c.596G>A