Canonical Allele Identifier: PA645494232
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319448
ClinVar RCV Id: RCV000355684 RCV001782812 RCV001812846 RCV002522859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Pro545Leu
CA8051599
NM_022162.3:c.1634C>T