Canonical Allele Identifier: PA2573278232
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396175
ClinVar RCV Id: RCV002555240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val358Gly
CA395868166
NM_022162.3:c.1073T>G