Canonical Allele Identifier: PA2825615182
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2937220
ClinVar RCV Id: RCV003791410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2531Ser
CA369219688
NM_001127487.2:c.7591A>T
CA369219695
NM_001127487.2:c.7592C>G