ClinGen Allele Registry
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Canonical Allele Identifier:
PA341852
Gene: FLNB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
34140
ClinVar RCV:
RCV000020451
ClinVar Variation:
21288
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001448.2:p.Ala1643Ser
CA341851
NM_001457.4:c.4927G>T