Canonical Allele Identifier: PA2580450895
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420388
ClinVar RCV Id: RCV003118913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Pro527His
CA395869215
NM_022162.3:c.1580C>A