Canonical Allele Identifier: PA2825070111
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2006694
ClinVar RCV Id: RCV002837875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Phe287Ser
CA404319287
NM_000159.4:c.860T>C