Canonical Allele Identifier: PA2580113721
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2107813
ClinVar RCV Id: RCV003033827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ala4Val
CA382032912
NM_000372.5:c.11C>T