Canonical Allele Identifier: PA107285
Gene: PYGL HGNC NCBI
ClinVar RCV:
RCV000031853
ClinVar Variation:
38367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Asn339Ser
CA342908
NM_002863.5:c.1016A>G