Canonical Allele Identifier: PA095219
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 286241
ClinVar RCV Id: RCV000521789 RCV000674015 RCV003409413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala382Thr
CA9234619
NM_000159.4:c.1144G>A