Canonical Allele Identifier: PA100963
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3806
ClinVar RCV Id: RCV000004010 RCV000085960 RCV003488322
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Leu216Met
CA227576
NM_000372.5:c.646T>A