Canonical Allele Identifier: PA915995520
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 644762
ClinVar RCV Id: RCV000798750 RCV004027966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Cys31Ser
CA371663332
NM_002485.5:c.92G>C
CA371663336
NM_002485.5:c.91T>A