Canonical Allele Identifier: PA2825615192
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2091588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asn2537Thr
CA369219774
NM_001127487.2:c.7610A>C