Canonical Allele Identifier: PA2741884895
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2565521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe1433Leu
CA4475307
NM_001458.5:c.4297T>C
CA369201081
NM_001458.5:c.4299C>A
CA369201083
NM_001458.5:c.4299C>G