Canonical Allele Identifier: PA2825614311
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1403390
ClinVar RCV Id: RCV001909028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Asn2035Ser
CA4475906
NM_001127487.2:c.6104A>G