Allele Registry

Canonical Allele Identifier: PA100558

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000085896

RCV001588916

ClinVar Variation:

99534

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asn371Tyr	CA227498 NM_000372.5:c.1111A>T