Canonical Allele Identifier: PA2580458350
Gene: SLC13A3 HGNC NCBI
ClinVar RCV:
RCV002574602
ClinVar Variation:
2173422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073740.2:p.Arg307Trp
CA9891482
NM_022829.6:c.919A>T