Allele Registry

Canonical Allele Identifier: PA100527

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000085933

RCV000414815

RCV003467006

ClinVar Variation:

99553

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Arg77Trp	CA227542 NM_000372.5:c.229C>T