Canonical Allele Identifier: PA101323
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99556
ClinVar RCV Id: RCV000085937 RCV004529899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Trp80Arg
CA227548
NM_000372.5:c.238T>C
CA382033863
NM_000372.5:c.238T>A