Allele Registry

Canonical Allele Identifier: PA645395646

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000021078

RCV000241867

RCV000710270

RCV003633482

ClinVar Variation:

21866

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Val81Met	CA342583 NM_000360.3:c.241G>A