Canonical Allele Identifier: PA2826050219
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161291.1:p.Cys209Arg
CA121565
NM_001167819.1:c.625T>C