Canonical Allele Identifier: PA658670186
Gene: ARHGAP32 HGNC NCBI

Linked Data

ClinVar Variation Id: 487793
ClinVar RCV Id: RCV000577845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136157.1:p.Thr1568Ser
CA383256908
NM_001142685.2:c.4703C>G
CA383256910
NM_001142685.2:c.4702A>T