Canonical Allele Identifier: PA2826835448
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4699
ClinVar RCV Id: RCV000416482 RCV003764528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Asp355Glu
CA117027
NM_001293557.2:c.1065C>G
CA395868321
NM_001293557.2:c.1065C>A