Canonical Allele Identifier: PA238895
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 193371
ClinVar RCV Id: RCV000536292 RCV000724177 RCV000987931 RCV001163311 RCV001272105 RCV001331839 RCV002470789 RCV003155104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055066.1:p.Met1Thr