Canonical Allele Identifier: PA2825614006
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg1898His
CA369208463
NM_001127487.2:c.5693G>A