Canonical Allele Identifier: PA2580262879
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2091588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asn2570Thr
CA369219774
NM_001458.5:c.7709A>C