Canonical Allele Identifier: PA2580364777
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2415198
ClinVar RCV Id: RCV003110617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Thr193Pro
CA404318159
NM_013976.3:c.577A>C
CA2580096510
NM_013976.3:c.576_577delinsAC