Canonical Allele Identifier: PA2573315852
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1412641
ClinVar RCV Id: RCV001923354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala1351Val
CA1395843
NM_206933.4:c.4052C>T