Canonical Allele Identifier: PA2827498373
Gene: ARHGAP26 HGNC NCBI

Linked Data

ClinVar Variation Id: 133543
ClinVar RCV Id: RCV000120056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336476.1:p.Thr574Ile
CA156904
NM_001349547.2:c.1721C>T