Canonical Allele Identifier: PA645429478
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 342654
ClinVar RCV Id: RCV000900427 RCV002520071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Thr679Ile
CA2553952
NM_020754.4:c.2036C>T