Canonical Allele Identifier: PA100435
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3796
ClinVar RCV Id: RCV000004000 RCV000085979 RCV000755072 RCV003156055 RCV003460423 RCV003492282 RCV003488321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Arg299His
CA227600
NM_000372.5:c.896G>A