Canonical Allele Identifier: PA2825334679
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469291
ClinVar RCV Id: RCV001993863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met214Val
CA371658202
NM_001024688.3:c.640A>G