Canonical Allele Identifier: PA2580113744
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2192740
ClinVar RCV Id: RCV002643810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Thr88Ser
CA6221074
NM_000372.5:c.262A>T
CA382033992
NM_000372.5:c.263C>G