Canonical Allele Identifier: PA2825964929
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1470202
ClinVar RCV Id: RCV001964068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157412.1:p.Tyr747His
CA389680723
NM_001163940.2:c.2239T>C