Allele Registry

Canonical Allele Identifier: PA2825335155

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000131458

RCV000199946

RCV000212747

RCV000735122

RCV002225444

RCV003492622

RCV003905237

ClinVar Variation:

142374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Thr370Pro	CA294382 NM_001024688.3:c.1108A>C