Canonical Allele Identifier: PA2580429780
Gene: SLC25A19 HGNC NCBI
ClinVar RCV:
RCV002719848
ClinVar Variation:
2394315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068380.3:p.Ser302Leu
CA8760864
NM_021734.5:c.905C>T