Canonical Allele Identifier: PA2825335435
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1777164
ClinVar RCV Id: RCV002394989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys467Asn
CA371655407
NM_001024688.3:c.1401A>T
CA371655408
NM_001024688.3:c.1401A>C