Canonical Allele Identifier: PA2573102076
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 557316
ClinVar RCV Id: RCV000673442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr2898Ser
CA344851511
NM_206933.4:c.8693A>C