Canonical Allele Identifier: PA2828432770
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_001357395.1:p.Asp355Glu
CA117027
NM_001370466.1:c.1065C>G
CA395868321
NM_001370466.1:c.1065C>A