Canonical Allele Identifier: PA2825335963
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 627828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.His651Asp
CA371674815
NM_001024688.3:c.1951C>G