Canonical Allele Identifier: PA156905
Gene: ARHGAP26 HGNC NCBI

Linked Data

ClinVar Variation Id: 133543
ClinVar RCV Id: RCV000120056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055886.1:p.Thr610Ile
CA156904
NM_015071.6:c.1829C>T