Canonical Allele Identifier: PA2573217719
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1488185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala1118Val
CA4475021
NM_001458.5:c.3353C>T