Canonical Allele Identifier: PA2573315739
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1396332
ClinVar RCV Id: RCV001902956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ile916Val
CA1396178
NM_206933.4:c.2746A>G