Canonical Allele Identifier: PA916028080
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543399
ClinVar RCV Id: RCV000654153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Ser53Ile
CA384356252
NM_001330374.1:c.158G>T