Canonical Allele Identifier: PA150313
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97869
ClinVar RCV Id: RCV000374813 RCV001529388 RCV000755646 RCV001811397 RCV001781428 RCV002260988 RCV002514482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val955Ile
CA150311
NM_022162.3:c.2863G>A