Canonical Allele Identifier: PA2825613192
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 864174
ClinVar RCV Id: RCV001071297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr1514Met
CA369201977
NM_001127487.2:c.4541C>T