Canonical Allele Identifier: PA658671944
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 483977
ClinVar RCV Id: RCV000566671 RCV003617832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Phe523Leu
CA371655573
NM_002485.5:c.1569T>G
CA371655574
NM_002485.5:c.1569T>A
CA371655579
NM_002485.5:c.1567T>C