Canonical Allele Identifier: PA645429521
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053047
ClinVar RCV Id: RCV002918976 RCV002937913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Leu833Phe
CA2554052
NM_020754.4:c.2497C>T