Canonical Allele Identifier: PA2573316669
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1469637
ClinVar RCV Id: RCV001961671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val4190Ala
CA37413100
NM_206933.4:c.12569T>C