Canonical Allele Identifier: PA658676650
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459952
ClinVar RCV Id: RCV000530261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ser246Leu
CA9234477
NM_000159.4:c.737C>T