Canonical Allele Identifier: PA2825613124
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 766888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val1487Met
CA4475350
NM_001127487.2:c.4459G>A