Canonical Allele Identifier: PA2828933919
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3026589
ClinVar RCV Id: RCV003886982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371057.1:p.Leu430Phe
CA384361156
NM_001384128.1:c.1288C>T