Canonical Allele Identifier: PA2827341150
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 469631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317588.1:p.Asn208Asp
CA10525125
NM_001330659.2:c.622A>G