Canonical Allele Identifier: PA2825619882
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2162573
ClinVar RCV Id: RCV003070310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119594.1:p.Arg320His
CA8760856
NM_001126122.2:c.959G>A