Canonical Allele Identifier: PA1139762956
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 166506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Met1344Val
CA179566
NM_206933.4:c.4030A>G