Canonical Allele Identifier: PA916009213
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Glu365Lys
CA252098
NM_013976.3:c.1093G>A