Canonical Allele Identifier: PA2829689206
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1403318
ClinVar RCV Id: RCV001908991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Pro746Ala
CA344865478
NM_007123.6:c.2236C>G