Canonical Allele Identifier: PA2828735673
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_001364954.1:p.Thr1528Ser
CA383256908
NM_001378025.1:c.4583C>G
CA383256910
NM_001378025.1:c.4582A>T