Canonical Allele Identifier: PA2573102063
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 438025
ClinVar RCV Id: RCV000504635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val2453Asp
CA344850058
NM_206933.4:c.7358T>A