Canonical Allele Identifier: PA2825614484
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539403
ClinVar RCV Id: RCV000649133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Cys2121Ser
CA369212589
NM_001127487.2:c.6361T>A
CA369212593
NM_001127487.2:c.6362G>C