Canonical Allele Identifier: PA2828933273
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141629
ClinVar RCV Id: RCV003074001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371055.1:p.Glu550Asp
CA384361044
NM_001384126.1:c.1650A>C
CA384361045
NM_001384126.1:c.1650A>T