Canonical Allele Identifier: PA150282
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97856
ClinVar RCV Id: RCV000280478 RCV000336827 RCV001781424 RCV002260984 RCV002513883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asn852Ser
CA150280
NM_022162.3:c.2555A>G