Canonical Allele Identifier: PA2825612561
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2929837
ClinVar RCV Id: RCV003785003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val1235Leu
CA369197759
NM_001127487.2:c.3703G>C
CA369197761
NM_001127487.2:c.3703G>T