Canonical Allele Identifier: PA2825614250
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1408552
ClinVar RCV Id: RCV001910021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Gly2006Arg
CA369211275
NM_001127487.2:c.6016G>A
CA369211277
NM_001127487.2:c.6016G>C