Canonical Allele Identifier: PA2825334670
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1764631
ClinVar RCV Id: RCV002373645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ile211Leu
CA371658254
NM_001024688.3:c.631A>T
CA371658255
NM_001024688.3:c.631A>C