Allele Registry

Canonical Allele Identifier: PA645498087

Gene: SLC27A5 HGNC NCBI

ClinVar Variation Id: 286343

HGVS (amino-acid)	Matching Registered Transcripts
NP_036386.1:p.Arg53Trp	CA9718338 NM_012254.3:c.157C>T