Canonical Allele Identifier: PA2826179036
Gene: SLC13A3 HGNC NCBI
ClinVar RCV:
RCV002659043
ClinVar Variation:
1946620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180268.1:p.Pro527Leu
CA409257351
NM_001193339.2:c.1580C>T