Canonical Allele Identifier: PA2829689885
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 418534
ClinVar RCV Id: RCV000484519 RCV000599950 RCV002222521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ser1136Arg
CA16617061
NM_007123.6:c.3408T>A
CA344868773
NM_007123.6:c.3408T>G
CA344868783
NM_007123.6:c.3406A>C