Canonical Allele Identifier: PA100713
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 11985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Arg515Ser
CA341167
NM_000170.3:c.1545G>C
CA372893274
NM_000170.3:c.1545G>T