Canonical Allele Identifier: PA1139762802
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 959826
ClinVar RCV Id: RCV001233244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg1135Gly
CA344868795
NM_206933.4:c.3403A>G