Canonical Allele Identifier: PA220427
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 92526
ClinVar RCV Id: RCV000078247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Asn374Asp
CA220426
NM_000159.4:c.1120A>G