ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826835901
Gene: NOD2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000320195
RCV001509517
RCV001781426
RCV002260986
RCV002513885
RCV003964950
ClinVar Variation:
97866
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001280486.1:p.Ala891Asp
CA150302
NM_001293557.2:c.2672C>A