Canonical Allele Identifier: PA645394559
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 425426
ClinVar RCV Id: RCV000487754 RCV002323848 RCV001368325 RCV003150239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1099Ile
CA4475012
NM_001458.5:c.3295G>A