Allele Registry

Canonical Allele Identifier: PA106102

Gene: FHL1 HGNC NCBI

ClinVar Allele:

26592

ClinVar RCV:

RCV000012309

RCV003511981

ClinVar Variation:

11553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153174.1:p.Cys153Tyr	CA121550 NM_001159702.2:c.458G>A