Allele Registry

Canonical Allele Identifier: PA116044

Gene: TPH2 HGNC NCBI

ClinVar RCV:

RCV000003314

RCV001113238

RCV002476916

ClinVar Variation:

3164

HGVS (amino-acid)	Matching Registered Transcripts
NP_775489.2:p.Pro206Ser	CA116043 NM_173353.4:c.616C>T