Canonical Allele Identifier: PA2573280278
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370320
ClinVar RCV Id: RCV001877104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Ala750Asp
CA354050050
NM_020754.4:c.2249C>A