Canonical Allele Identifier: PA2573226684
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1463348
ClinVar RCV Id: RCV001997683 RCV002398019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val580Gly
CA371655201
NM_002485.5:c.1739T>G