Canonical Allele Identifier: PA2825304955
Gene: SLC13A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2891165
ClinVar RCV Id: RCV003722839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011554.1:p.Leu18Arg
CA315749411
NM_001011554.3:c.53T>G