Canonical Allele Identifier: PA2828405357
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414873
ClinVar RCV Id: RCV000757290 RCV001079716 RCV001173489 RCV001283349 RCV002446876 RCV003960079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357227.2:p.Thr216Ile
CA6506604
NM_001370298.3:c.647C>T