Canonical Allele Identifier: PA100986
Gene: FGF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 13837
ClinVar RCV Id: RCV000014849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005238.1:p.Ser156Pro
CA341306
NM_005247.4:c.466T>C