Allele Registry

Canonical Allele Identifier: PA101340

Gene: TYR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

18812

ClinVar RCV:

RCV000003972

RCV000085973

RCV000192471

RCV000778348

RCV001542595

RCV002476919

RCV004532280

ClinVar Variation:

3773

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Val275Phe	CA227591 NM_000372.5:c.823G>T