Canonical Allele Identifier: PA1139764773
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 180064
ClinVar RCV Id: RCV000156867 RCV000666306 RCV001278867 RCV003453203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr3986Ala
CA185733
NM_206933.4:c.11956A>G