Canonical Allele Identifier: PA2825615198
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2953528
ClinVar RCV Id: RCV003812751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys2543Asn
CA369219857
NM_001127487.2:c.7629G>C
CA369219859
NM_001127487.2:c.7629G>T