Canonical Allele Identifier: PA2825613106
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala1475Val
CA4475329
NM_001127487.2:c.4424C>T