Canonical Allele Identifier: PA2825614225
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1314338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.His1990Arg
CA369211143
NM_001127487.2:c.5969A>G