Canonical Allele Identifier: PA118447
Gene: FAAH HGNC NCBI

Linked Data

ClinVar Variation Id: 6724
ClinVar RCV Id: RCV000007116 RCV002496290 RCV003974803
JSON-LD

Amino-acid Alleles

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