Canonical Allele Identifier: PA2825334660
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1446553
ClinVar RCV Id: RCV001958530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln209His
CA371658274
NM_001024688.3:c.627G>T
CA371658277
NM_001024688.3:c.627G>C