Canonical Allele Identifier: PA150210
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97831
ClinVar RCV Id: RCV000084088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Trp490Leu
CA150208
NM_022162.3:c.1469G>T