Canonical Allele Identifier: PA915986132
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 361010
ClinVar RCV Id: RCV000271327 RCV000593765 RCV001277318 RCV000328760 RCV003168565 RCV001095212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Gly650Arg
CA4352738
NM_001160210.2:c.1948G>C
CA368257229
NM_001160210.2:c.1948G>A