Canonical Allele Identifier: PA2825334490
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1025023
ClinVar RCV Id: RCV001325281 RCV002366200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys154Asn
CA371658891
NM_001024688.3:c.462G>T
CA371658892
NM_001024688.3:c.462G>C