Canonical Allele Identifier: PA2825611117
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val601Ala
CA4474480
NM_001127487.2:c.1802T>C