Canonical Allele Identifier: PA121567
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11557
ClinVar RCV Id: RCV000012313 RCV003511982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001440.2:p.Cys209Arg
CA121565
NM_001449.4:c.625T>C