Canonical Allele Identifier: PA658809027
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539337
ClinVar RCV Id: RCV000649064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro2565Ser
CA369219703
NM_001458.5:c.7693C>T