Canonical Allele Identifier: PA645479863
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 288248
ClinVar RCV Id: RCV000284260 RCV000671394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ser119Leu
CA10606016
NM_000159.4:c.356C>T