Canonical Allele Identifier: PA1139707661
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 910781
ClinVar RCV Id: RCV001162815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp629Gly
CA371677238
NM_002485.5:c.1886A>G