Allele Registry

Canonical Allele Identifier: PA100858

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

18840

ClinVar RCV:

RCV000004005

RCV000085920

RCV000602413

RCV002496250

RCV003325937

RCV003466803

RCV004540988

ClinVar Variation:

3801

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Gly446Ser	CA227525 NM_000372.5:c.1336G>A