Canonical Allele Identifier: PA2826893638
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3026589
ClinVar RCV Id: RCV003886982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291412.1:p.Leu182Phe
CA384361156
NM_001304483.2:c.544C>T