Allele Registry

Canonical Allele Identifier: PA100688

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003993

RCV000085930

RCV000763288

RCV000778345

RCV002288461

RCV003466801

ClinVar Variation:

3790

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Cys55Tyr	CA227538 NM_000372.5:c.164G>A