Canonical Allele Identifier: PA2825070026
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1498017
ClinVar RCV Id: RCV001996365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg227Leu
CA404318600
NM_000159.4:c.680G>T