Canonical Allele Identifier: PA2573280279
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503852
ClinVar RCV Id: RCV002045533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Ala763Pro
CA81697499
NM_020754.4:c.2287G>C