Canonical Allele Identifier: PA658808042
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 542454
ClinVar RCV Id: RCV000652877 RCV001592827 RCV002343377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620128.1:p.Ala18Ser
CA3364464
NM_138773.4:c.52G>T