Canonical Allele Identifier: PA2580567921
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2173781
ClinVar RCV Id: RCV002584731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gln3561Arg
CA37437375
NM_206933.4:c.10682A>G