Canonical Allele Identifier: PA2573102098
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1306306
ClinVar RCV Id: RCV001767259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr3585Ile
CA344834452
NM_206933.4:c.10754C>T