Canonical Allele Identifier: PA2825334228
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 480024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met1Ile
CA371662480
NM_001024688.3:c.3G>T
CA371662481
NM_001024688.3:c.3G>C
CA371662482
NM_001024688.3:c.3G>A