Canonical Allele Identifier: PA645394544
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 430130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp646His
CA4474534
NM_001458.5:c.1936G>C