Canonical Allele Identifier: PA2825334225
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 483961
ClinVar RCV Id: RCV000570692 RCV000636702 RCV003322792 RCV003465240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met1Leu