Canonical Allele Identifier: PA2825070005
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1706404
ClinVar RCV Id: RCV002284934 RCV003464435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Pro217Leu
CA404318490
NM_000159.4:c.650C>T