Canonical Allele Identifier: PA2499305552
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1047736
ClinVar RCV Id: RCV001352493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Leu4132Pro
CA1393473
NM_206933.4:c.12395T>C