Canonical Allele Identifier: PA1139764585
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 179843
ClinVar RCV Id: RCV000156642 RCV000763828 RCV001271141 RCV002516341 RCV003888605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr3635Asn
CA185250
NM_206933.4:c.10904C>A