Canonical Allele Identifier: PA2828432630
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319431
ClinVar RCV Id: RCV000585590 RCV001121630 RCV001782795 RCV002263011 RCV002521021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Thr162Met
CA8051320
NM_001370466.1:c.485C>T