Canonical Allele Identifier: PA1139707411
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 962991
ClinVar RCV Id: RCV001236947 RCV003353243
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp577Val
CA371655223
NM_002485.5:c.1730A>T