Allele Registry

Canonical Allele Identifier: PA100311

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003994

RCV000085958

RCV003460419

ClinVar Variation:

3791

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Ala206Thr	CA227574 NM_000372.5:c.616G>A