Canonical Allele Identifier: PA110510
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4699
ClinVar RCV Id: RCV000416482 RCV003764528
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asp382Glu
CA117027
NM_022162.3:c.1146C>G
CA395868321
NM_022162.3:c.1146C>A