Canonical Allele Identifier: PA095492
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu365Lys
CA252098
NM_000159.4:c.1093G>A