Canonical Allele Identifier: PA2741816464
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2679410
ClinVar RCV Id: RCV003464766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Gln273His
CA6221198
NM_000372.5:c.819G>T
CA382035661
NM_000372.5:c.819G>C