Canonical Allele Identifier: PA2828432979
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319452
ClinVar RCV Id: RCV000293577 RCV000385541 RCV002521035 RCV003972363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala585Ser
CA8051634
NM_001370466.1:c.1753G>T