Canonical Allele Identifier: PA192299
Gene: NBN HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Phe262Leu
CA192297
NM_002485.5:c.786C>A
CA371658650
NM_002485.5:c.786C>G
CA371658658
NM_002485.5:c.784T>C