Canonical Allele Identifier: PA658678448
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 471987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val586Ala
CA4474467
NM_001458.5:c.1757T>C