Canonical Allele Identifier: PA2499277330
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1299668
ClinVar RCV Id: RCV001730140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly268Val
CA9234495
NM_013976.3:c.803G>T