Allele Registry

Canonical Allele Identifier: PA104941

Gene: TPH2 HGNC NCBI

ClinVar RCV:

RCV000003313

ClinVar Variation:

3163

HGVS (amino-acid)	Matching Registered Transcripts
NP_775489.2:p.Arg303Trp	CA116042 NM_173353.4:c.907C>T