Allele Registry

Canonical Allele Identifier: PA100646

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000004006

RCV000085921

ClinVar Variation:

3802

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asp448Asn	CA227526 NM_000372.5:c.1342G>A