Canonical Allele Identifier: PA2825614236
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 853788
ClinVar RCV Id: RCV001058670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro2002Leu
CA369211243
NM_001127487.2:c.6005C>T