Canonical Allele Identifier: PA2580276602
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1764631
ClinVar RCV Id: RCV002373645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ile293Leu
CA371658254
NM_002485.5:c.877A>T
CA371658255
NM_002485.5:c.877A>C