Canonical Allele Identifier: PA150192
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97826
ClinVar RCV Id: RCV000084081 RCV000954297 RCV001781414 RCV002262677 RCV002514472 RCV003974994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser431Leu
CA150190
NM_022162.3:c.1292C>T