Canonical Allele Identifier: PA150230
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97838
ClinVar RCV Id: RCV000084095 RCV001092928 RCV002514475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg587Cys
CA150228
NM_022162.3:c.1759C>T