Canonical Allele Identifier: PA2825964903
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 998113
ClinVar RCV Id: RCV001293800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Gly652Arg
CA389682467
NM_001163940.2:c.1954G>C
CA389682468
NM_001163940.2:c.1954G>A