Canonical Allele Identifier: PA915985778
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11555
ClinVar RCV Id: RCV000012311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153173.1:p.Cys133Arg
CA121555
NM_001159701.2:c.397T>C