Canonical Allele Identifier: PA2580168967
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 2236824
ClinVar RCV Id: RCV002718847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Met2472Thr
CA353334861
NM_001164317.2:c.7415T>C