Canonical Allele Identifier: PA2573102041
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 550393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr1357Met
CA1395839
NM_206933.4:c.4070C>T