Canonical Allele Identifier: PA2829689841
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ser1122Ala
CA143461
NM_007123.6:c.3364T>G