Canonical Allele Identifier: PA2580113747
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1996044
ClinVar RCV Id: RCV002801757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys91Arg
CA382034033
NM_000372.5:c.271T>C