Canonical Allele Identifier: PA2825070060
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2264917
ClinVar RCV Id: RCV002808471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala247Gly
CA404318788
NM_000159.4:c.740C>G