Canonical Allele Identifier: PA148167
Gene: FGD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 95092
ClinVar RCV Id: RCV000081097 RCV000514781 RCV000608756 RCV002313779 RCV003905060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004454.2:p.Arg132Gln
CA148166
NM_004463.3:c.395G>A