Canonical Allele Identifier: PA2573316663
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1374675
ClinVar RCV Id: RCV001900661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn4182Lys
CA344850669
NM_206933.4:c.12546T>G
CA344850670
NM_206933.4:c.12546T>A