Canonical Allele Identifier: PA2829953314
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128747
ClinVar RCV Id: RCV004422631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Glu687Gln
CA354048724
NM_020754.4:c.2059G>C