Canonical Allele Identifier: PA916074820
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 660383
ClinVar RCV Id: RCV000817564
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Glu171Gly
CA397749976
NM_177550.5:c.512A>G