Canonical Allele Identifier: PA2742037463
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3028661
ClinVar RCV Id: RCV003890526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro4155Ser
CA344850845
NM_206933.4:c.12463C>T