Canonical Allele Identifier: PA2826835972
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319475
ClinVar RCV Id: RCV000295535 RCV001782836 RCV002522869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gly1005Ser
CA8052076
NM_001293557.2:c.3013G>A