Canonical Allele Identifier: PA2825934789
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153176.1:p.Thr152Ser
CA414608567
NM_001159704.1:c.454A>T
CA414608569
NM_001159704.1:c.455C>G