Canonical Allele Identifier: PA196896
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_002476.2:p.Met294Leu
CA196894
NM_002485.5:c.880A>T
CA371658245
NM_002485.5:c.880A>C