Canonical Allele Identifier: PA1139762771
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 961960
ClinVar RCV Id: RCV001235728 RCV001834048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn1071Ser
CA1396050
NM_206933.4:c.3212A>G