Canonical Allele Identifier: PA2580566923
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2202968
ClinVar RCV Id: RCV002634345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro1320Leu
CA344867102
NM_206933.4:c.3959C>T