Canonical Allele Identifier: PA2825335313
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 480021
ClinVar RCV Id: RCV000565151 RCV002225668 RCV000792565
ClinVar Variation Id: 1000422
ClinVar RCV Id: RCV001296546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asn421Lys
CA371655706
NM_001024688.3:c.1263T>G
CA371655707
NM_001024688.3:c.1263T>A