Allele Registry

Canonical Allele Identifier: PA101118

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

18811

ClinVar RCV:

RCV000003970

RCV000085939

RCV000505170

RCV000599844

RCV000623980

RCV001249700

RCV002496249

RCV003387499

RCV003466799

RCV003993735

ClinVar Variation:

3772

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Pro81Leu	CA227551 NM_000372.5:c.242C>T