Canonical Allele Identifier: PA2741976168
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2936815
ClinVar RCV Id: RCV003799053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Thr509Ser
CA395869109
NM_022162.3:c.1525A>T
CA395869110
NM_022162.3:c.1526C>G