Canonical Allele Identifier: PA891858045
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 570678
ClinVar RCV Id: RCV000691592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Ala704Thr
CA260821502
NM_002863.5:c.2110G>A