Canonical Allele Identifier: PA645403466
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 239008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001440.2:p.Ser130Gly
CA10583932
NM_001449.4:c.388A>G