Canonical Allele Identifier: PA2573168880
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1458819
ClinVar RCV Id: RCV001949604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.His202Gln
CA6221152
NM_000372.5:c.606T>G
CA382034932
NM_000372.5:c.606T>A