Canonical Allele Identifier: PA2829830679
Gene: UPF2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056357.1:p.Phe591Ile
CA375993742
NM_015542.4:c.1771T>A