Canonical Allele Identifier: PA2580568617
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1949670
ClinVar RCV Id: RCV002676394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Trp4657Arg
CA344840980
NM_206933.4:c.13969T>C
CA344840981
NM_206933.4:c.13969T>A