Canonical Allele Identifier: PA2825858272
Gene: SLC13A5 HGNC NCBI
ClinVar RCV:
RCV003013810
ClinVar Variation:
2095478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Phe495Ser
CA397737073
NM_001143838.3:c.1484T>C