Canonical Allele Identifier: PA2573168909
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1360996
ClinVar RCV Id: RCV001865091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asp228Asn
CA226290694
NM_000372.5:c.682G>A