Canonical Allele Identifier: PA150356
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97885
ClinVar RCV Id: RCV000178335 RCV000369785 RCV000768031 RCV001781434 RCV002514491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg311Trp
CA150354
NM_022162.3:c.931C>T