Canonical Allele Identifier: PA095723
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 557741
ClinVar RCV Id: RCV000673919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Thr429Met
CA9234696
NM_000159.4:c.1286C>T