Canonical Allele Identifier: PA2828318500
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410318
ClinVar RCV Id: RCV000462272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356260.1:p.Gly145dup
CA16616636
NM_001369331.1:c.434_436dup