Canonical Allele Identifier: PA2742037443
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2505676
ClinVar RCV Id: RCV003235908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Glu3911Asp
CA1393625
NM_206933.4:c.11733G>T
CA344829819
NM_206933.4:c.11733G>C