Canonical Allele Identifier: PA2825613188
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2928802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Tyr1513His
CA369201967
NM_001127487.2:c.4537T>C