Canonical Allele Identifier: PA2580113770
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1694644
ClinVar RCV Id: RCV002262364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ile246Phe
CA382035247
NM_000372.5:c.736A>T