Allele Registry

Canonical Allele Identifier: PA061526

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000202401

ClinVar Variation:

218174

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