Allele Registry

Canonical Allele Identifier: PA126562

Gene: FABP2 HGNC NCBI

ClinVar RCV:

RCV000017958

RCV001650835

ClinVar Variation:

16494

HGVS (amino-acid)	Matching Registered Transcripts
NP_000125.2:p.Thr55Ala	CA126561 NM_000134.4:c.163A>G