Canonical Allele Identifier: PA658828128
Gene: FGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 545461
ClinVar RCV Id: RCV000656428 RCV001007891 RCV003767888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149354.1:p.Arg44Trp
CA5657679
NM_033164.4:c.130C>T