Canonical Allele Identifier: PA2825335793
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 219546
ClinVar RCV Id: RCV000204839 RCV000220088 RCV000505926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gly598Ser
CA349023
NM_001024688.3:c.1792G>A