Allele Registry

Canonical Allele Identifier: PA100339

Gene: TYR HGNC NCBI

ClinVar RCV:

RCV000195157

RCV000778350

RCV001853121

RCV003462302

ClinVar Variation:

212520

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Ala355Val	CA277447 NM_000372.5:c.1064C>T