Canonical Allele Identifier: PA2741816436
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2679408
ClinVar RCV Id: RCV003464765 RCV003553974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Pro81Ser
CA6221067
NM_000372.5:c.241C>T