Canonical Allele Identifier: PA658806901
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 501915
ClinVar RCV Id: RCV000595168 RCV002532630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068380.3:p.Ala254Val
CA8760896
NM_021734.5:c.761C>T