Canonical Allele Identifier: PA2573074607
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_001364953.1:p.Thr1582Ser
CA383256908
NM_001378024.1:c.4745C>G
CA383256910
NM_001378024.1:c.4744A>T