Canonical Allele Identifier: PA2825964796
Gene: PYGL HGNC NCBI
ClinVar RCV:
RCV000020504
ClinVar Variation:
21339
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Amino-acid Alleles

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