Canonical Allele Identifier: PA2825611219
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1489987
ClinVar RCV Id: RCV001978455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ile643Leu
CA369227379
NM_001127487.2:c.1927A>C