Canonical Allele Identifier: PA2829689876
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48501
ClinVar RCV Id: RCV000041827 RCV001061173 RCV001831703 RCV003450840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg1135Ser
CA143463
NM_007123.6:c.3405G>C
CA344868787
NM_007123.6:c.3405G>T