Canonical Allele Identifier: PA2573226041
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1470202
ClinVar RCV Id: RCV001964068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Tyr781His
CA389680723
NM_002863.5:c.2341T>C