Canonical Allele Identifier: PA2825335728
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 141979
ClinVar RCV Id: RCV000130735 RCV000543794 RCV001547889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu576Gly
CA167004
NM_001024688.3:c.1727A>G