Canonical Allele Identifier: PA2825964888
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 21330
ClinVar RCV Id: RCV000020495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Asn598Ile
CA341910
NM_001163940.2:c.1793A>T