Canonical Allele Identifier: PA2573077232
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 662801
ClinVar RCV Id: RCV000820538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371055.1:p.Met701Ile
CA384367593
NM_001384126.1:c.2103G>A
CA384367596
NM_001384126.1:c.2103G>C
CA384367599
NM_001384126.1:c.2103G>T