Canonical Allele Identifier: PA2825611614
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 579440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asn824Tyr
CA369191694
NM_001127487.2:c.2470A>T