Allele Registry

Canonical Allele Identifier: PA100623

Gene: TYR HGNC NCBI

ClinVar Allele:

18828

ClinVar RCV:

RCV000003992

RCV000085915

ClinVar Variation:

3789

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asp42Gly	CA227521 NM_000372.5:c.125A>G