Canonical Allele Identifier: PA2573280289
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407793
ClinVar RCV Id: RCV001918625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Thr789Ala
CA2554019
NM_020754.4:c.2365A>G