Canonical Allele Identifier: PA658678712
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2578Ser
CA4476342
NM_001458.5:c.7732G>A