Canonical Allele Identifier: PA341927
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 21339
ClinVar RCV Id: RCV000020504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Gly233Asp
CA341926
NM_002863.5:c.698G>A