Canonical Allele Identifier: PA2826692764
Gene: SLC13A5 HGNC NCBI
ClinVar RCV:
RCV001045389
ClinVar Variation:
842888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Val520Met
CA397736781
NM_001284510.2:c.1558G>A