Canonical Allele Identifier: PA2825335461
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 461518
ClinVar RCV Id: RCV000538636 RCV000566431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ile476Leu
CA371655351
NM_001024688.3:c.1426A>T
CA371655352
NM_001024688.3:c.1426A>C