Canonical Allele Identifier: PA915986115
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 6007
ClinVar RCV Id: RCV000006376 RCV000728351 RCV001267011 RCV001831517 RCV002508184 RCV003581555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Arg589Gln
CA253676
NM_001160210.2:c.1766G>A