Allele Registry

Canonical Allele Identifier: PA3057552160

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV005006743

ClinVar Variation:

3574114

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Arg217Pro	CA382035052 NM_000372.5:c.650G>C