Canonical Allele Identifier: PA645429509
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 288159
ClinVar RCV Id: RCV000313938 RCV003137897 RCV003930148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Gly775Ser
CA2554008
NM_020754.4:c.2323G>A