Canonical Allele Identifier: PA2825615237
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714613
ClinVar RCV Id: RCV002295704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Glu2579Asp
CA369220128
NM_001127487.2:c.7737G>C
CA369220130
NM_001127487.2:c.7737G>T