Canonical Allele Identifier: PA658808130
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 499592
ClinVar RCV Id: RCV000592650 RCV002532472
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055066.1:p.Gly561Arg
CA4352819
NM_014251.3:c.1681G>A
CA368258218
NM_014251.3:c.1681G>C