Canonical Allele Identifier: PA149947
Gene: NLRP7 HGNC NCBI

Linked Data

ClinVar Variation Id: 97715
ClinVar RCV Id: RCV000083968 RCV000991059 RCV003221803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120727.1:p.Lys379Asn
CA149945
NM_001127255.1:c.1137G>C
CA407862580
NM_001127255.1:c.1137G>T