Canonical Allele Identifier: PA2825612495
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472041
ClinVar RCV Id: RCV000556230 RCV002307543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly1197Arg
CA4475074
NM_001127487.2:c.3589G>A
CA369197300
NM_001127487.2:c.3589G>C