Canonical Allele Identifier: PA2829011991
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Asn212Ser
CA6506682
NM_001385118.1:c.635A>G