Canonical Allele Identifier: PA2828317072
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646065
ClinVar RCV Id: RCV000800282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356255.1:p.Phe127Leu
CA414608390
NM_001369326.1:c.379T>C
CA414608395
NM_001369326.1:c.381C>A
CA414608396
NM_001369326.1:c.381C>G