Canonical Allele Identifier: PA2825611162
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 576189
ClinVar RCV Id: RCV000698623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asp620His
CA369227227
NM_001127487.2:c.1858G>C