Canonical Allele Identifier: PA2825934902
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537349
ClinVar RCV Id: RCV000646180 RCV002422346 RCV003144423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153176.1:p.Gln268His
CA336096760
NM_001159704.1:c.804G>C
CA414609877
NM_001159704.1:c.804G>T