Canonical Allele Identifier: PA150171
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97819
ClinVar RCV Id: RCV000084073 RCV002513868 RCV001781412 RCV001811395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asp357Ala
CA150169
NM_022162.3:c.1070A>C