Canonical Allele Identifier: PA915986109
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 499592
ClinVar RCV Id: RCV000592650 RCV002532472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Gly562Arg
CA4352819
NM_001160210.2:c.1684G>A
CA368258218
NM_001160210.2:c.1684G>C