Canonical Allele Identifier: PA2826692066
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675654
ClinVar RCV Id: RCV002211383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Gly209Arg
CA8331651
NM_001284509.2:c.625G>A
CA397748820
NM_001284509.2:c.625G>C