Canonical Allele Identifier: PA2825611248
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1311883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala661Thr
CA369227497
NM_001127487.2:c.1981G>A