Canonical Allele Identifier: PA2827939153
Gene: NOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201018
ClinVar RCV Id: RCV004487885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341778.1:p.Val144Leu
CA4205201
NM_001354849.2:c.430G>T
CA367135564
NM_001354849.2:c.430G>C