Canonical Allele Identifier: PA2741976171
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2934753
ClinVar RCV Id: RCV003798455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly534Asp
CA395869253
NM_022162.3:c.1601G>A