Canonical Allele Identifier: PA2580262883
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_001449.3:p.Glu2612Asp
CA369220128
NM_001458.5:c.7836G>C
CA369220130
NM_001458.5:c.7836G>T