Canonical Allele Identifier: PA2741976027
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937622
ClinVar RCV Id: RCV003794252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Met152Ile
CA395866753
NM_022162.3:c.456G>A
CA395866755
NM_022162.3:c.456G>C
CA395866756
NM_022162.3:c.456G>T