Canonical Allele Identifier: PA645479856
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 418224
ClinVar RCV Id: RCV000485466 RCV000675080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg94Gln
CA9234312
NM_000159.4:c.281G>A