Canonical Allele Identifier: PA150195
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97827
ClinVar RCV Id: RCV000084082 RCV000658746 RCV001781415 RCV002513869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu441Lys
CA150193
NM_022162.3:c.1321G>A