Canonical Allele Identifier: PA2825334648
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1763951
ClinVar RCV Id: RCV002447930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln204His
CA371658358
NM_001024688.3:c.612G>T
CA371658361
NM_001024688.3:c.612G>C