Canonical Allele Identifier: PA101290
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99577
ClinVar RCV Id: RCV000085967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Trp236Ser
CA227585
NM_000372.5:c.707G>C