Allele Registry

Canonical Allele Identifier: PA915962527

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000851370

RCV002533981

ClinVar Variation:

627594

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Gly53Cys	CA382033587 NM_000372.5:c.157G>T