Allele Registry

Canonical Allele Identifier: PA100572

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003989

RCV000085902

RCV003460416

ClinVar Variation:

3786

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asn382Lys	CA227506 NM_000372.5:c.1146C>A CA382028856 NM_000372.5:c.1146C>G