Canonical Allele Identifier: PA2825615160
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 848269
ClinVar RCV Id: RCV001051989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gln2516His
CA4476332
NM_001127487.2:c.7548G>T
CA369219505
NM_001127487.2:c.7548G>C