Canonical Allele Identifier: PA2573168795
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1444715
ClinVar RCV Id: RCV001982559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ser79Trp
CA382033858
NM_000372.5:c.236C>G