Canonical Allele Identifier: PA2741825908
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2696621
ClinVar RCV Id: RCV003507608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ala45Tyr
CA2697550009
NM_001024688.3:c.133_134delinsTA