Canonical Allele Identifier: PA2825612094
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472031
ClinVar RCV Id: RCV000547281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Met1029Val
CA4474948
NM_001127487.2:c.3085A>G