Canonical Allele Identifier: PA1139764758
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 855869
ClinVar RCV Id: RCV001061214
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala3922Thr
CA1393622
NM_206933.4:c.11764G>A