Canonical Allele Identifier: PA2573176722
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1407831
ClinVar RCV Id: RCV001937888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Phe24Leu
CA371662255
NM_001024688.3:c.72C>G
CA371662256
NM_001024688.3:c.72C>A
CA371662265
NM_001024688.3:c.70T>C