Canonical Allele Identifier: PA2826701152
Gene: ARHGAP30 HGNC NCBI

Linked Data

ClinVar Variation Id: 2477277
ClinVar RCV Id: RCV004269288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274529.1:p.Ala683Val
CA1204105
NM_001287600.2:c.2048C>T