Canonical Allele Identifier: PA2825611240
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 290012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Leu659Arg
CA4474541
NM_001127487.2:c.1976T>G