Canonical Allele Identifier: PA1139763820
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 969874
ClinVar RCV Id: RCV001245314 RCV001835234 RCV004034820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gly2561Arg
CA1394765
NM_206933.4:c.7681G>A
CA344841074
NM_206933.4:c.7681G>C