Canonical Allele Identifier: PA2826178974
Gene: SLC13A3 HGNC NCBI
ClinVar RCV:
RCV002574602
ClinVar Variation:
2173422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180268.1:p.Arg257Trp
CA9891482
NM_001193339.2:c.769A>T