Canonical Allele Identifier: PA2825070049
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1000110
ClinVar RCV Id: RCV001296197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Glu239Lys
CA404318712
NM_000159.4:c.715G>A