Canonical Allele Identifier: PA2580416605
Gene: SLC25A38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2016873
ClinVar RCV Id: RCV002851796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060345.2:p.Thr243Ile
CA352205350
NM_017875.4:c.728C>T