Canonical Allele Identifier: PA2580458385
Gene: SLC13A3 HGNC NCBI
ClinVar RCV:
RCV002659043
ClinVar Variation:
1946620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073740.2:p.Pro577Leu
CA409257351
NM_022829.6:c.1730C>T