Allele Registry

Canonical Allele Identifier: PA100477

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000004004

RCV000085911

RCV003387715

RCV003466802

RCV003557662

ClinVar Variation:

3800

2735735

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Arg403Ser	CA227516 NM_000372.5:c.1209G>T CA382077867 NM_000372.5:c.1209G>C