Canonical Allele Identifier: PA1139762526
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 958765
ClinVar RCV Id: RCV001231985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gly774Arg
CA344865088
NM_206933.4:c.2320G>C
CA344865090
NM_206933.4:c.2320G>A