Canonical Allele Identifier: PA645466034
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 230687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Leu574Val
CA10578754
NM_002485.5:c.1720T>G