Canonical Allele Identifier: PA2573094312
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307795
ClinVar RCV Id: RCV001772650 RCV002540325 RCV003401683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Glu805Val
CA2554034
NM_020754.4:c.2414A>T