Canonical Allele Identifier: PA658820182
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 499152
ClinVar RCV Id: RCV000593125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Arg151Gln
CA2553590
NM_020754.4:c.452G>A