Canonical Allele Identifier: PA2741816441
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2735722
ClinVar RCV Id: RCV003557652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Lys142Met
CA6221105
NM_000372.5:c.425A>T