Canonical Allele Identifier: PA2825611749
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 936351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly876Val
CA166176275
NM_001127487.2:c.2627G>T