Canonical Allele Identifier: PA2828317996
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401197
ClinVar RCV Id: RCV001896871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356258.1:p.Tyr240Ser
CA414609660
NM_001369329.1:c.719A>C