Canonical Allele Identifier: PA1139757894
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 842888
ClinVar RCV Id: RCV001045389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Val563Met
CA397736781
NM_177550.5:c.1687G>A