Canonical Allele Identifier: PA915988243
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 6399
ClinVar RCV Id: RCV000030661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Gly1617Arg
CA130017
NM_001164317.2:c.4849G>A
CA353352098
NM_001164317.2:c.4849G>C