Canonical Allele Identifier: PA2825614553
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2632681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ser2149Gly
CA369212787
NM_001127487.2:c.6445A>G