Canonical Allele Identifier: PA2741884718
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2947137
ClinVar RCV Id: RCV003801327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2044Leu
CA369211346
NM_001458.5:c.6130G>T
CA369211348
NM_001458.5:c.6130G>C