Canonical Allele Identifier: PA2573217721
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1450050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala1136Val
CA4475031
NM_001458.5:c.3407C>T