Canonical Allele Identifier: PA658693756
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 493101
ClinVar RCV Id: RCV000585060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asp448_Tyr451del
CA658683693
NM_000372.5:c.1342_1353del