Canonical Allele Identifier: PA658676622
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459949
ClinVar RCV Id: RCV000533495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu90Lys
CA305500200
NM_000159.4:c.268G>A