Canonical Allele Identifier: PA2741965828
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 2631617
ClinVar RCV Id: RCV003397392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Arg814_Thr815delinsSerSer
CA2695199265
NM_020754.4:c.2442_2443delinsTT