ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825335080
Gene: NBN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
485920
ClinVar RCV Id:
RCV000569911
RCV001054209
RCV002491138
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001019859.1:p.Pro345Thr
CA371656207
NM_001024688.3:c.1033C>A