Canonical Allele Identifier: PA2826893695
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 38444
ClinVar RCV Id: RCV000032000
ClinVar Variation Id: 637078
ClinVar RCV Id: RCV000789101 RCV003447169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291412.1:p.Met318Ile
CA384367648
NM_001304483.2:c.954G>A
CA384367652
NM_001304483.2:c.954G>C
CA384367653
NM_001304483.2:c.954G>T