Canonical Allele Identifier: PA2825069999
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 862517
ClinVar RCV Id: RCV001069251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Asn215Asp
CA404318460
NM_000159.4:c.643A>G