Canonical Allele Identifier: PA2825964910
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1029650
ClinVar RCV Id: RCV001330994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Gly661Arg
CA7183226
NM_001163940.2:c.1981G>A
CA389682372
NM_001163940.2:c.1981G>C