Allele Registry

Canonical Allele Identifier: PA118447

Gene: FAAH HGNC NCBI

ClinVar RCV:

RCV000007116

RCV002496290

RCV003974803

ClinVar Variation:

6724

HGVS (amino-acid)	Matching Registered Transcripts
NP_001432.2:p.Pro129Thr	CA118446 NM_001441.3:c.385C>A