Canonical Allele Identifier: PA2826701234
Gene: ARHGAP30 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128740
ClinVar RCV Id: RCV004422624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274531.1:p.Cys736Ser
CA343320237
NM_001287602.2:c.2207G>C
CA343320239
NM_001287602.2:c.2206T>A