Canonical Allele Identifier: PA2499286568
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049744
ClinVar RCV Id: RCV001356244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Gly772Arg
CA2554005
NM_020754.4:c.2314G>A
CA354050479
NM_020754.4:c.2314G>C