Canonical Allele Identifier: PA095198
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2083
ClinVar RCV Id: RCV000002164 RCV000790796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala293Thr
CA234085
NM_000159.4:c.877G>A