Canonical Allele Identifier: PA263355
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Pro765Ser
CA263353
NM_000170.3:c.2293C>T