Canonical Allele Identifier: PA1139762642
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 842442
ClinVar RCV Id: RCV001044868 RCV001827277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr907Ile
CA37501070
NM_206933.4:c.2720C>T