Canonical Allele Identifier: PA2825334673
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 421530
ClinVar RCV Id: RCV000478839 RCV001036229 RCV002446933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met212Thr
CA4802879
NM_001024688.3:c.635T>C