Canonical Allele Identifier: PA2580276598
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1763951
ClinVar RCV Id: RCV002447930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln286His
CA371658358
NM_002485.5:c.858G>T
CA371658361
NM_002485.5:c.858G>C