Canonical Allele Identifier: PA2580568152
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2094193
ClinVar RCV Id: RCV003021218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Lys4022Asn
CA37395085
NM_206933.4:c.12066G>T
CA344826698
NM_206933.4:c.12066G>C