Canonical Allele Identifier: PA2825335270
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 663144
ClinVar RCV Id: RCV000820960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Leu408Phe
CA371655787
NM_001024688.3:c.1224A>T
CA371655788
NM_001024688.3:c.1224A>C