Canonical Allele Identifier: PA2825612358
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2943186
ClinVar RCV Id: RCV003800304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Phe1135Leu
CA369196756
NM_001127487.2:c.3403T>C
CA369196763
NM_001127487.2:c.3405T>A
CA369196765
NM_001127487.2:c.3405T>G