Allele Registry

Canonical Allele Identifier: PA116041

Gene: TPH2 HGNC NCBI

ClinVar RCV:

RCV000003312

ClinVar Variation:

3162

HGVS (amino-acid)	Matching Registered Transcripts
NP_775489.2:p.Arg441His	CA116040 NM_173353.4:c.1322G>A