Allele Registry

Canonical Allele Identifier: PA100711

Gene: TYR HGNC NCBI

ClinVar Allele:

48497

ClinVar RCV:

RCV000033111

RCV002513316

RCV003466887

ClinVar Variation:

39977

HGVS (amino-acid)	Matching Registered Transcripts
NP_000363.1:p.Cys91Tyr	CA261236 NM_000372.5:c.272G>A