Canonical Allele Identifier: PA2825612301
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1034548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala1105Ser
CA4475016
NM_001127487.2:c.3313G>T