Canonical Allele Identifier: PA2573077239
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 623800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371055.1:p.Ala711Val
CA384367854
NM_001384126.1:c.2132C>T