Canonical Allele Identifier: PA2573217918
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1405385
ClinVar RCV Id: RCV001903763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro2725Leu
CA369222275
NM_001458.5:c.8174C>T