Canonical Allele Identifier: PA2825335465
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 993117
ClinVar RCV Id: RCV001284190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu477Asp
CA371655340
NM_001024688.3:c.1431A>T
CA371655341
NM_001024688.3:c.1431A>C