Canonical Allele Identifier: PA2828432850
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1306492
ClinVar RCV Id: RCV001770672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Glu435Asp
CA395868823
NM_001370466.1:c.1305G>T
CA395868824
NM_001370466.1:c.1305G>C