Canonical Allele Identifier: PA1139762809
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 418534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ser1136Arg
CA16617061
NM_206933.4:c.3408T>A
CA344868773
NM_206933.4:c.3408T>G
CA344868783
NM_206933.4:c.3406A>C