Canonical Allele Identifier: PA2828317749
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356257.1:p.Ala322Pro
CA351843
NM_001369328.1:c.964G>C