Allele Registry

Canonical Allele Identifier: PA116439

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000003978

RCV000003979

RCV000003980

RCV000003981

RCV000003982

RCV000085910

RCV000254054

RCV000500466

RCV000626673

RCV000721172

RCV001269379

RCV003985252

ClinVar Variation:

3779

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Arg402Gln	CA116438 NM_000372.5:c.1205G>A