Canonical Allele Identifier: PA2825611226
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 430130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp646His
CA4474534
NM_001127487.2:c.1936G>C