Canonical Allele Identifier: PA2741816439
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2633321
ClinVar RCV Id: RCV004529270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys91Phe
CA382034038
NM_000372.5:c.272G>T