Allele Registry

Canonical Allele Identifier: PA101290

Gene: TYR HGNC NCBI

ClinVar Allele:

105466

ClinVar RCV:

RCV000085967

ClinVar Variation:

99577

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Trp236Ser	CA227585 NM_000372.5:c.707G>C