Canonical Allele Identifier: PA915986094
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 252921
ClinVar RCV Id: RCV000239389 RCV000595565 RCV001163201 RCV002057271 RCV003475850 RCV003909878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Pro503Leu
CA4352889
NM_001160210.2:c.1508C>T