Allele Registry

Canonical Allele Identifier: PA101095

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000003976

RCV000085913

RCV000400442

RCV000500113

RCV000623187

RCV000762872

RCV001375218

RCV001813946

RCV003460414

RCV004532283

ClinVar Variation:

3777

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Pro406Leu	CA227519 NM_000372.5:c.1217C>T