Canonical Allele Identifier: PA1139745916
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838660
ClinVar RCV Id: RCV001040250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly380Asp
CA395868306
NM_022162.3:c.1139G>A