Canonical Allele Identifier: PA2573102097
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 444199
ClinVar RCV Id: RCV000512654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr3565His
CA344836370
NM_206933.4:c.10693T>C