Canonical Allele Identifier: PA166978
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 141971
ClinVar RCV Id: RCV000130718 RCV001338002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp525Glu
CA166976
NM_002485.5:c.1575T>A
CA371655560
NM_002485.5:c.1575T>G