Canonical Allele Identifier: PA1139762645
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 991453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro909His
CA1396179
NM_206933.4:c.2726C>A