Canonical Allele Identifier: PA658678605
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 450485
ClinVar RCV Id: RCV000522128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1920Leu
CA4475774
NM_001458.5:c.5759C>T