Canonical Allele Identifier: PA1139762811
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 991451
ClinVar RCV Id: RCV001279667 RCV001871575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val1137Ile
CA37504940
NM_206933.4:c.3409G>A