Canonical Allele Identifier: PA2825614293
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 861277
ClinVar RCV Id: RCV002355091 RCV001067770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly2021Arg
CA369211469
NM_001127487.2:c.6061G>A
CA369211472
NM_001127487.2:c.6061G>C