Canonical Allele Identifier: PA095712
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2084
ClinVar RCV Id: RCV000002165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Thr416Ile
CA252096
NM_000159.4:c.1247C>T