Canonical Allele Identifier: PA645494256
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319457
ClinVar RCV Id: RCV000361829 RCV001812849 RCV001782819 RCV002521037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Leu682Phe
CA8051681
NM_022162.3:c.2046G>T
CA395870683
NM_022162.3:c.2046G>C