Canonical Allele Identifier: PA1139688070
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 910988
ClinVar RCV Id: RCV001163198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Tyr609Cys
CA4352775
NM_001160210.2:c.1826A>G