Canonical Allele Identifier: PA2826002290
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 2435338
ClinVar RCV Id: RCV003135190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Ala688Thr
CA6079547
NM_001164716.1:c.2062G>A