Canonical Allele Identifier: PA2827024150
Gene: FHL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222639
ClinVar RCV Id: RCV000208406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305827.1:p.Phe125Val
CA353997
NM_001318898.2:c.373T>G