Canonical Allele Identifier: PA2573217846
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1466392
ClinVar RCV Id: RCV001966070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Met2167Val
CA369212694
NM_001458.5:c.6499A>G