Canonical Allele Identifier: PA1139702980
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 860132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Glu1104Lys
CA4475015
NM_001458.5:c.3310G>A