Canonical Allele Identifier: PA2826472582
Gene: ARHGAP20 HGNC NCBI

Linked Data

ClinVar Variation Id: 161737
ClinVar RCV Id: RCV000149273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245345.1:p.Val129Ala
CA174694
NM_001258416.2:c.386T>C