Allele Registry

Canonical Allele Identifier: PA116437

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003977

RCV000055807

RCV000085955

RCV000173114

RCV000341159

RCV004527285

ClinVar Variation:

3778

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Ser192Tyr	CA116436 NM_000372.5:c.575C>A