Allele Registry

Canonical Allele Identifier: PA100435

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000004000

RCV000085979

RCV000755072

RCV003156055

RCV003460423

RCV003488321

RCV003492282

ClinVar Variation:

3796

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Arg299His	CA227600 NM_000372.5:c.896G>A