Canonical Allele Identifier: PA2830099746
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722901
ClinVar RCV Id: RCV002306008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149353.1:p.Pro26Arg
CA377838462
NM_033163.4:c.77C>G