Canonical Allele Identifier: PA2580262823
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2143831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Phe2225Leu
CA369213094
NM_001458.5:c.6673T>C
CA369213104
NM_001458.5:c.6675C>A
CA369213106
NM_001458.5:c.6675C>G