Canonical Allele Identifier: PA2825070062
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1304015
ClinVar RCV Id: RCV001758308 RCV004526141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ile250Thr
CA404318819
NM_000159.4:c.749T>C