Canonical Allele Identifier: PA2580276609
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2136686
ClinVar RCV Id: RCV003058200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Leu297Phe
CA371658183
NM_002485.5:c.889C>T