Canonical Allele Identifier: PA2499305645
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1215648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ser1349Phe
CA1395844
NM_206933.4:c.4046C>T