Canonical Allele Identifier: PA2825334237
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 925449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ser6Phe
CA371662447
NM_001024688.3:c.17C>T