Canonical Allele Identifier: PA2580267171
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2333038
ClinVar RCV Id: RCV002930558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002854.3:p.Tyr53His
CA389699431
NM_002863.5:c.157T>C