Canonical Allele Identifier: PA2580429038
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 2300929
ClinVar RCV Id: RCV002850456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Ser689Ile
CA354048820
NM_020754.4:c.2066G>T