Canonical Allele Identifier: PA274332
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 189063
ClinVar RCV Id: RCV000169460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg128Gln
CA274331
NM_000159.4:c.383G>A