Canonical Allele Identifier: PA2825335973
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 231721
ClinVar RCV Id: RCV000220264 RCV001303812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu655Asp
CA10578742
NM_001024688.3:c.1965G>T
CA371674783
NM_001024688.3:c.1965G>C