Canonical Allele Identifier: PA106083
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11551
ClinVar RCV Id: RCV000012307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153174.1:p.Cys132Phe
CA121546
NM_001159702.2:c.395G>T