Canonical Allele Identifier: PA106002
Gene: SLC25A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 18246
ClinVar RCV Id: RCV000019908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001142.2:p.Val289Met
CA127985
NM_001151.4:c.865G>A