Canonical Allele Identifier: PA2573101652
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 295437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn760Ser
CA1396255
NM_206933.4:c.2279A>G