Canonical Allele Identifier: PA353998
Gene: FHL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222639
ClinVar RCV Id: RCV000208406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963849.1:p.Phe239Val
CA353997
NM_201555.3:c.715T>G