Canonical Allele Identifier: PA645479766
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330031
ClinVar RCV Id: RCV000645634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653288.1:p.Pro450Leu
CA9639446
NM_144687.4:c.1349C>T