Canonical Allele Identifier: PA2580429015
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071281
ClinVar RCV Id: RCV002949269 RCV002975457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Ala423Pro
CA2553789
NM_020754.4:c.1267G>C