Canonical Allele Identifier: PA2825964762
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2538269
ClinVar RCV Id: RCV003256484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Cys79Tyr
CA7183887
NM_001163940.2:c.236G>A