Canonical Allele Identifier: PA2573226617
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 836214
ClinVar RCV Id: RCV001037286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asn521_Leu522insTyr
CA916080402
NM_002485.5:c.1562_1564dup