Canonical Allele Identifier: PA2580568110
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1909574
ClinVar RCV Id: RCV002587476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gly3921Glu
CA344829590
NM_206933.4:c.11762G>A