Canonical Allele Identifier: PA2826835383
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97883
ClinVar RCV Id: RCV000084140 RCV002225284 RCV002260990 RCV001781433 RCV002513889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Thr267Ser
CA150348
NM_001293557.2:c.800C>G
CA395867764
NM_001293557.2:c.799A>T