Canonical Allele Identifier: PA2825069963
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1705686
ClinVar RCV Id: RCV002284000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Met191Arg
CA404318138
NM_000159.4:c.572T>G