Canonical Allele Identifier: PA095613
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2736819
ClinVar RCV Id: RCV003497354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Leu309Trp
CA404319538
NM_000159.4:c.926T>G