Canonical Allele Identifier: PA110501
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97842
ClinVar RCV Id: RCV000084099 RCV002513874
ClinVar Variation Id: 623348
ClinVar RCV Id: RCV000761493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asn670Lys
CA150239
NM_022162.3:c.2010C>A
CA395870549
NM_022162.3:c.2010C>G