Canonical Allele Identifier: PA2573255984
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1416120
ClinVar RCV Id: RCV001935537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Asp230Asn
CA305500646
NM_013976.3:c.688G>A