Canonical Allele Identifier: PA2825335366
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 483977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Phe441Leu
CA371655573
NM_001024688.3:c.1323T>G
CA371655574
NM_001024688.3:c.1323T>A
CA371655579
NM_001024688.3:c.1321T>C