Canonical Allele Identifier: PA2828318457
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11555
ClinVar RCV Id: RCV000012311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356260.1:p.Cys104Arg
CA121555
NM_001369331.1:c.310T>C