Canonical Allele Identifier: PA2741884795
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2951619
ClinVar RCV Id: RCV003812306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Met2669Ile
CA369221083
NM_001458.5:c.8007G>A
CA369221084
NM_001458.5:c.8007G>C
CA369221085
NM_001458.5:c.8007G>T