Canonical Allele Identifier: PA915995671
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 663236
ClinVar RCV Id: RCV000821079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu62Asp
CA371662611
NM_002485.5:c.186A>T
CA371662612
NM_002485.5:c.186A>C