Canonical Allele Identifier: PA2825614522
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1753987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg2140His
CA369212737
NM_001127487.2:c.6419G>A