Canonical Allele Identifier: PA1139730006
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 930605
ClinVar RCV Id: RCV001196391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Pro804Gln
CA354051093
NM_020754.4:c.2411C>A