Canonical Allele Identifier: PA254663
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9126
ClinVar RCV Id: RCV000009697 RCV000988442 RCV001531080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.Thr229Met
CA254662
NM_033163.4:c.686C>T