Allele Registry

Canonical Allele Identifier: PA342584

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000021078

RCV000241867

RCV000710270

RCV003633482

ClinVar Variation:

21866

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Val112Met	CA342583 NM_199292.3:c.334G>A