Canonical Allele Identifier: PA340496
Gene: SLC25A15 HGNC NCBI

Linked Data

ClinVar Variation Id: 6000
ClinVar RCV Id: RCV000006366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055067.1:p.Thr32Arg
CA340495
NM_014252.4:c.95C>G