Canonical Allele Identifier: PA061526
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 218174
ClinVar RCV Id: RCV000202401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Asp524His
CA279908
NM_177550.5:c.1570G>C