Canonical Allele Identifier: PA2573280296
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1683707
ClinVar RCV Id: RCV002244228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Ser824Phe
CA354051474
NM_020754.4:c.2471C>T