Canonical Allele Identifier: PA351606
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 221907
ClinVar RCV Id: RCV000207408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Thr344Ile
CA351605
NM_000159.4:c.1031C>T