Canonical Allele Identifier: PA2573101869
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 156393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gly805Ala
CA270788
NM_206933.4:c.2414G>C