Canonical Allele Identifier: PA341919
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 21335
ClinVar RCV Id: RCV000020500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Lys681Thr
CA341918
NM_002863.5:c.2042A>C