Allele Registry

Canonical Allele Identifier: PA100548

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000004002

RCV000085897

RCV004526588

ClinVar Variation:

3798

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asn371Thr	CA227499 NM_000372.5:c.1112A>C