Canonical Allele Identifier: PA2573315889
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1368706
ClinVar RCV Id: RCV001874475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg1521Cys
CA1395692
NM_206933.4:c.4561C>T