Canonical Allele Identifier: PA2828432960
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97838
ClinVar RCV Id: RCV000084095 RCV001092928 RCV002514475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg560Cys
CA150228
NM_001370466.1:c.1678C>T