Canonical Allele Identifier: PA2573278093
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374340
ClinVar RCV Id: RCV002552137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Pro177Ala
CA395866998
NM_022162.3:c.529C>G