Canonical Allele Identifier: PA2580365095
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1995265
ClinVar RCV Id: RCV002796465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Met405Thr
CA404321807
NM_013976.3:c.1214T>C