Canonical Allele Identifier: PA2827308410
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2177823
ClinVar RCV Id: RCV002588376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Asp52Val
CA384356245
NM_001330374.1:c.155A>T
CA2580085358
NM_001330374.1:c.155_156delinsTT