Allele Registry

Canonical Allele Identifier: PA645419770

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000478390

ClinVar Variation:

422828

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Phe269del	CA16619416 NM_000372.5:c.806_808del