Canonical Allele Identifier: PA645415799
Gene: ARHGAP24 HGNC NCBI

Linked Data

ClinVar Variation Id: 384543
ClinVar RCV Id: RCV000441338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020787.2:p.Gly742Glu
CA2994919
NM_001025616.3:c.2225G>A