Canonical Allele Identifier: PA2742037469
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2757915
ClinVar RCV Id: RCV003569448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala4246Asp
CA344849477
NM_206933.4:c.12737C>A