Canonical Allele Identifier: PA094152
Gene: SLC25A15 HGNC NCBI

Linked Data

ClinVar Variation Id: 5997
ClinVar RCV Id: RCV000006363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055067.1:p.Met37Arg
CA340492
NM_014252.4:c.110T>G