Canonical Allele Identifier: PA1139745929
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956780
ClinVar RCV Id: RCV002563167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser402Phe
CA8051493
NM_022162.3:c.1205C>T