Canonical Allele Identifier: PA100527
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99553
ClinVar RCV Id: RCV000085933 RCV000414815 RCV003467006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Arg77Trp
CA227542
NM_000372.5:c.229C>T