Canonical Allele Identifier: PA341927
Gene: PYGL HGNC NCBI
ClinVar RCV:
RCV000020504
ClinVar Variation:
21339
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Amino-acid Alleles

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