Canonical Allele Identifier: PA2826002159
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 877372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Ile532Thr
CA6079693
NM_001164716.1:c.1595T>C