Canonical Allele Identifier: PA1139706247
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 925115
ClinVar RCV Id: RCV001224280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ile293Met
CA371658247
NM_002485.5:c.879A>G