Canonical Allele Identifier: PA916048338
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188310
ClinVar RCV Id: RCV000168307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Asn39His
CA334580
NM_001370297.1:c.115A>C