Canonical Allele Identifier: PA1139729151
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 971376
ClinVar RCV Id: RCV001247144 RCV001252002 RCV004034887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ala316Thr
CA9234551
NM_013976.3:c.946G>A