Canonical Allele Identifier: PA101302
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99581
ClinVar RCV Id: RCV000085971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Trp272Cys
CA227589
NM_000372.5:c.816G>C
CA382035654
NM_000372.5:c.816G>T