Canonical Allele Identifier: PA095752
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2088
ClinVar RCV Id: RCV000002169 RCV000224327 RCV002512671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val400Met
CA252099
NM_000159.4:c.1198G>A