Canonical Allele Identifier: PA2825614542
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539391
ClinVar RCV Id: RCV000649120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Phe2145Ser
CA369212763
NM_001127487.2:c.6434T>C