Canonical Allele Identifier: PA913201452
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 239008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153171.1:p.Ser146Gly
CA10583932
NM_001159699.2:c.436A>G