Canonical Allele Identifier: PA645394546
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 290012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Leu659Arg
CA4474541
NM_001458.5:c.1976T>G