Canonical Allele Identifier: PA2573102040
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 597787
ClinVar RCV Id: RCV000734013 RCV001075084 RCV001825481 RCV002307609 RCV002535362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val1339Gly
CA1395854
NM_206933.4:c.4016T>G