Canonical Allele Identifier: PA658808665
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539358
ClinVar RCV Id: RCV000649086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ser101Phe
CA369216950
NM_001458.5:c.302C>T