Canonical Allele Identifier: PA2825946380
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2180246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Arg284Cys
CA4353117
NM_001160210.2:c.850C>T