Canonical Allele Identifier: PA2830099833
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2117899
ClinVar RCV Id: RCV003053487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149354.1:p.Arg67Cys
CA377836989
NM_033164.4:c.199C>T