Canonical Allele Identifier: PA1139764722
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 866827
ClinVar RCV Id: RCV001075143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ile3844Val
CA344834578
NM_206933.4:c.11530A>G