Canonical Allele Identifier: PA1139745671
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 887101
ClinVar RCV Id: RCV001121629 RCV001784657 RCV002556554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Leu172Phe
CA395866970
NM_022162.3:c.516G>C
CA395866971
NM_022162.3:c.516G>T