Canonical Allele Identifier: PA2741816459
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2631170
ClinVar RCV Id: RCV004531547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys244Ser
CA6221184
NM_000372.5:c.731G>C
CA382035230
NM_000372.5:c.730T>A