Allele Registry

Canonical Allele Identifier: PA277152

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000193486

RCV003317144

ClinVar Variation:

212525

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Glu328Lys	CA277151 NM_000372.5:c.982G>A