Canonical Allele Identifier: PA645494300
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319471
ClinVar RCV Id: RCV000366842 RCV001782833 RCV002261066 RCV002521045 RCV003326408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gln902Lys
CA8051929
NM_022162.3:c.2704C>A