Canonical Allele Identifier: PA150213
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97832
ClinVar RCV Id: RCV000084089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Cys495Tyr
CA150211
NM_022162.3:c.1484G>A