Canonical Allele Identifier: PA105986
Gene: SLC25A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 18247
ClinVar RCV Id: RCV000019909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001142.2:p.Leu98Pro
CA127986
NM_001151.4:c.293T>C