Allele Registry

Canonical Allele Identifier: PA100870

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000003997

RCV000003998

RCV000085925

RCV000763287

RCV001267064

RCV003460421

RCV004532284

ClinVar Variation:

3794

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Gly47Asp	CA227531 NM_000372.5:c.140G>A