Canonical Allele Identifier: PA2830099750
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2672413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.Arg28Ser
CA5657688
NM_033163.4:c.84G>T
CA377838379
NM_033163.4:c.84G>C