Canonical Allele Identifier: PA2826572403
Gene: NLRP12 HGNC NCBI
ClinVar RCV:
RCV000645634
ClinVar Variation:
330031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Pro450Leu
CA9639446
NM_001277126.2:c.1349C>T