Allele Registry

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Canonical Allele Identifier: PA2826691912

Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515117

ClinVar RCV Id: RCV002020855

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271438.1:p.Arg37Ser	CA397752058 NM_001284509.2:c.111G>T CA397752061 NM_001284509.2:c.111G>C