Canonical Allele Identifier: PA254659
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9122
ClinVar RCV Id: RCV000009692 RCV000239300 RCV000767027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.Pro26Leu
CA254658
NM_033163.4:c.77C>T