Canonical Allele Identifier: PA645429517
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 342658
ClinVar RCV Id: RCV000454849 RCV001522002 RCV001554024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Gly803Ser
CA2554030
NM_020754.4:c.2407G>A