Allele Registry

Canonical Allele Identifier: PA100611

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000003974

RCV000085903

RCV000680155

RCV000755077

RCV000762870

RCV001266635

RCV003230346

RCV003460413

RCV004532281

ClinVar Variation:

3775

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Asp383Asn	CA227507 NM_000372.5:c.1147G>A