Canonical Allele Identifier: PA2825614546
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg2147Pro
CA369212776
NM_001127487.2:c.6440G>C