Canonical Allele Identifier: PA2827939176
Gene: NOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201004
ClinVar RCV Id: RCV004487871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341778.1:p.Thr429Ser
CA367133079
NM_001354849.2:c.1286C>G
CA367133082
NM_001354849.2:c.1285A>T