Canonical Allele Identifier: PA1139705073
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 848269
ClinVar RCV Id: RCV001051989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gln2549His
CA4476332
NM_001458.5:c.7647G>T
CA369219505
NM_001458.5:c.7647G>C