Canonical Allele Identifier: PA2580567503
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2155313
ClinVar RCV Id: RCV003083848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr2897Ala
CA1394534
NM_206933.4:c.8689A>G