Canonical Allele Identifier: PA2825615184
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539337
ClinVar RCV Id: RCV000649064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro2532Ser
CA369219703
NM_001127487.2:c.7594C>T