Canonical Allele Identifier: PA2828318038
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356258.1:p.Tyr272Phe
CA10525137
NM_001369329.1:c.815A>T