Canonical Allele Identifier: PA246798
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 198249
ClinVar RCV Id: RCV000179520 RCV003333036 RCV004020148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068380.3:p.Ala189Thr
CA246797
NM_021734.5:c.565G>A