Canonical Allele Identifier: PA094137
Gene: SLC25A15 HGNC NCBI

Linked Data

ClinVar Variation Id: 5998
ClinVar RCV Id: RCV000006364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055067.1:p.Leu71Gln
CA340493
NM_014252.4:c.212T>A