Canonical Allele Identifier: PA2825334429
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 481832
ClinVar RCV Id: RCV000562538 RCV001034793 RCV002222555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gly132Arg
CA371659161
NM_001024688.3:c.394G>C
CA371659163
NM_001024688.3:c.394G>A