Canonical Allele Identifier: PA1139705193
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 859047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Met2687Val
CA4476418
NM_001458.5:c.8059A>G