Canonical Allele Identifier: PA2828432552
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3068617
ClinVar RCV Id: RCV003994686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Phe47Leu
CA395865773
NM_001370466.1:c.139T>C
CA395865781
NM_001370466.1:c.141C>A
CA395865783
NM_001370466.1:c.141C>G