Canonical Allele Identifier: PA2825614088
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1023624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Lys1935Thr
CA4475829
NM_001127487.2:c.5804A>C