Canonical Allele Identifier: PA916046385
Gene: ARHGAP21 HGNC NCBI

Linked Data

ClinVar Variation Id: 402147
ClinVar RCV Id: RCV000454179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354384.1:p.Ile951Arg
CA16609524
NM_001367455.1:c.2852T>G