Canonical Allele Identifier: PA645477312
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 435186
ClinVar RCV Id: RCV000503695
ClinVar Variation Id: 2573738
ClinVar RCV Id: RCV003318074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.Ser87Arg
CA377836740
NM_033163.4:c.261C>G
CA377836741
NM_033163.4:c.261C>A
CA377836756
NM_033163.4:c.259A>C