Canonical Allele Identifier: PA2825614554
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 643027
ClinVar RCV Id: RCV000796628
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2151Ser
CA4476014
NM_001127487.2:c.6452C>G
CA369212803
NM_001127487.2:c.6451A>T