Canonical Allele Identifier: PA2825619705
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2162573
ClinVar RCV Id: RCV003070310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119593.1:p.Arg320His
CA8760856
NM_001126121.2:c.959G>A