Canonical Allele Identifier: PA2573278513
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413813
ClinVar RCV Id: RCV002557672 RCV002261420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Phe677Leu
CA8051676
NM_022162.3:c.2031C>G
CA395870621
NM_022162.3:c.2029T>C
CA395870630
NM_022162.3:c.2031C>A