Canonical Allele Identifier: PA2827307979
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015
ClinVar RCV Id: RCV000001070 RCV000789103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Met205Thr
CA339859
NM_001330373.1:c.614T>C