Canonical Allele Identifier: PA1139762655
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 805744
ClinVar RCV Id: RCV000993541 RCV003455013 RCV003455014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Leu921Met
CA1396173
NM_206933.4:c.2761C>A