Canonical Allele Identifier: PA645501995
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 392193
ClinVar RCV Id: RCV000442613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Thr7Ser
CA16607248
NM_001304481.1:c.20C>G
CA384354760
NM_001304481.1:c.19A>T