Canonical Allele Identifier: PA645426156
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 361014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055066.1:p.Gly465Cys
CA4352941
NM_014251.3:c.1393G>T