Canonical Allele Identifier: PA2573316591
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1449838
ClinVar RCV Id: RCV001989833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ser3996Cys
CA344827149
NM_206933.4:c.11987C>G