Canonical Allele Identifier: PA2573307699
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_808218.1:p.Gly226Arg
CA8331651
NM_177550.5:c.676G>A
CA397748820
NM_177550.5:c.676G>C