Canonical Allele Identifier: PA2827308683
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 38444
ClinVar RCV Id: RCV000032000
ClinVar Variation Id: 637078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Met473Ile
CA384367648
NM_001330374.1:c.1419G>A
CA384367652
NM_001330374.1:c.1419G>C
CA384367653
NM_001330374.1:c.1419G>T