Canonical Allele Identifier: PA2741884786
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2953528
ClinVar RCV Id: RCV003812751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2576Asn
CA369219857
NM_001458.5:c.7728G>C
CA369219859
NM_001458.5:c.7728G>T