Canonical Allele Identifier: PA2825256637
Gene: ARHGEF35 HGNC NCBI

Linked Data

ClinVar Variation Id: 2388732
ClinVar RCV Id: RCV004222839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003702.2:p.Met407Val
CA168140766
NM_001003702.3:c.1219A>G