Canonical Allele Identifier: PA2825070036
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1404269
ClinVar RCV Id: RCV001901565 RCV003490927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Cys228Phe
CA404318610
NM_000159.4:c.683G>T