Allele Registry

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Canonical Allele Identifier: PA2825334672

Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 187162

ClinVar RCV Id: RCV000166860 RCV000478151 RCV000545234

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Met212Leu	CA196894 NM_001024688.3:c.634A>T CA371658245 NM_001024688.3:c.634A>C