Canonical Allele Identifier: PA2580429047
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 2094678
ClinVar RCV Id: RCV003010374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Asp816Glu
CA354051335
NM_020754.4:c.2448T>A
CA354051338
NM_020754.4:c.2448T>G