Canonical Allele Identifier: PA2580493400
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1708951
ClinVar RCV Id: RCV002288235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.His93Arg
CA377836561
NM_033163.4:c.278A>G