Canonical Allele Identifier: PA2830256859
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 329998
ClinVar RCV Id: RCV000370362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653288.1:p.Arg1051Pro
CA9638746
NM_144687.4:c.3152G>C