Canonical Allele Identifier: PA2826001697
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 551114
ClinVar RCV Id: RCV000666086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Glu23_Val25del
CA658822244
NM_001164716.1:c.67_75del