Canonical Allele Identifier: PA915986127
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 203938
ClinVar RCV Id: RCV000270533 RCV000381101 RCV000726730 RCV000764738 RCV001095246 RCV001277319 RCV003967465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Val638Ala
CA312978
NM_001160210.2:c.1913T>C