Canonical Allele Identifier: PA2573316889
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1496365
ClinVar RCV Id: RCV001991840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Glu4963Gly
CA344827895
NM_206933.4:c.14888A>G