ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826835442
Gene: NOD2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
97902
ClinVar RCV Id:
RCV000084160
RCV002262685
RCV001753488
RCV002513891
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001280486.1:p.Arg346Cys
CA150374
NM_001293557.2:c.1036C>T