Canonical Allele Identifier: PA333489
Gene: UBE3A HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570853.1:p.Leu263Trp
CA333487
NM_130838.1:c.788T>G