Canonical Allele Identifier: PA658816562
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530764
ClinVar RCV Id: RCV000636779 RCV001525443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Thr273Ile
CA371658541
NM_002485.5:c.818C>T