Canonical Allele Identifier: PA2742037238
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3028737
ClinVar RCV Id: RCV003890602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn791Lys
CA1396241
NM_206933.4:c.2373T>G
CA344864937
NM_206933.4:c.2373T>A