Canonical Allele Identifier: PA2828432746
Gene: NOD2 HGNC NCBI
ClinVar RCV:
RCV000258859
ClinVar Variation:
268134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Leu322Phe
CA10602671
NM_001370466.1:c.964C>T