Canonical Allele Identifier: PA2827341153
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317588.1:p.Ala209Pro
CA351843
NM_001330659.2:c.625G>C