Canonical Allele Identifier: PA2827939155
Gene: NOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2334463
ClinVar RCV Id: RCV004173216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341778.1:p.Thr197Ser
CA367134893
NM_001354849.2:c.590C>G
CA367134897
NM_001354849.2:c.589A>T