Canonical Allele Identifier: PA915983751
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 650142
ClinVar RCV Id: RCV000805240 RCV002345806 RCV001567298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys1237Asn
CA4475104
NM_001458.5:c.3711A>C
CA369197794
NM_001458.5:c.3711A>T