Canonical Allele Identifier: PA115095
Gene: NLRP7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1593
ClinVar RCV Id: RCV000001660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120727.1:p.Pro651Ser
CA115093
NM_001127255.1:c.1951C>T