Canonical Allele Identifier: PA915996204
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 639981
ClinVar RCV Id: RCV000792912 RCV002442616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp284Gly
CA4802880
NM_002485.5:c.851A>G