Canonical Allele Identifier: PA2825612417
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1731753
ClinVar RCV Id: RCV002460259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val1158Leu
CA369197034
NM_001127487.2:c.3472G>C
CA369197036
NM_001127487.2:c.3472G>T