Allele Registry

Canonical Allele Identifier: PA645464265

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000484157

RCV000695139

RCV001184071

ClinVar Variation:

421151

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Met1Thr