Canonical Allele Identifier: PA150298
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97864
ClinVar RCV Id: RCV000084121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Trp907Arg
CA150296
NM_022162.3:c.2719T>C
CA395875000
NM_022162.3:c.2719T>A