Canonical Allele Identifier: PA2826692443
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 218174
ClinVar RCV Id: RCV000202401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Asp481His
CA279908
NM_001284510.2:c.1441G>C