Canonical Allele Identifier: PA1139764572
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 855225
ClinVar RCV Id: RCV001060442 RCV003467808 RCV003455273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.His3607Pro
CA1393914
NM_206933.4:c.10820A>C