Canonical Allele Identifier: PA150350
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97883
ClinVar RCV Id: RCV000084140 RCV002225284 RCV002260990 RCV001781433 RCV002513889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Thr294Ser
CA150348
NM_022162.3:c.881C>G
CA395867764
NM_022162.3:c.880A>T