Canonical Allele Identifier: PA2825619702
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 325065
ClinVar RCV Id: RCV000384560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119593.1:p.Phe310Leu
CA10650094
NM_001126121.2:c.930C>A
CA401001117
NM_001126121.2:c.930C>G
CA401001143
NM_001126121.2:c.928T>C