Canonical Allele Identifier: PA2573280241
Gene: ARHGAP31 HGNC NCBI
ClinVar RCV:
RCV001918523
ClinVar Variation:
1407584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Arg199Gln
CA2553642
NM_020754.4:c.596G>A