Canonical Allele Identifier: PA2828405211
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188396
ClinVar RCV Id: RCV000168459 RCV000357650 RCV000658641 RCV001094181 RCV001174114 RCV002399597 RCV003917576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Pro387Thr
CA346829
NM_001370297.1:c.1159C>A