Canonical Allele Identifier: PA2741975998
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2934952
ClinVar RCV Id: RCV003798654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly25Ala
CA395865146
NM_022162.3:c.74G>C