Canonical Allele Identifier: PA2826835687
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319455
ClinVar RCV Id: RCV000403955 RCV001782817 RCV002522863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ala634Pro
CA8051663
NM_001293557.2:c.1900G>C