Canonical Allele Identifier: PA645429359
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 283576
ClinVar RCV Id: RCV000281382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Thr116Met
CA2553526
NM_020754.4:c.347C>T