Canonical Allele Identifier: PA916020899
Gene: ARHGEF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 157538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295082.1:p.His757Tyr
CA270961
NM_001308153.1:c.2269C>T