Canonical Allele Identifier: PA913201441
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11555
ClinVar RCV Id: RCV000012311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153171.1:p.Cys120Arg
CA121555
NM_001159699.2:c.358T>C