Canonical Allele Identifier: PA2825858032
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 660383
ClinVar RCV Id: RCV000817564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Glu171Gly
CA397749976
NM_001143838.3:c.512A>G