Canonical Allele Identifier: PA2827307889
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 245808
ClinVar RCV Id: RCV000236896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Gly69Arg
CA6506640
NM_001330373.1:c.205G>C