Canonical Allele Identifier: PA915983986
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 766888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val1487Met
CA4475350
NM_001458.5:c.4459G>A