Canonical Allele Identifier: PA2580262881
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2591Arg
CA369219967
NM_001458.5:c.7772A>G