Allele Registry

Canonical Allele Identifier: PA645429449

Gene: TPH2 HGNC NCBI

ClinVar RCV:

RCV000334080

RCV002502215

ClinVar Variation:

310378

HGVS (amino-acid)	Matching Registered Transcripts
NP_775489.2:p.Ser41Tyr	CA6689674 NM_173353.4:c.122C>A