Canonical Allele Identifier: PA2580471362
Gene: ARHGAP39 HGNC NCBI
ClinVar Allele:
2220309
ClinVar RCV:
RCV004095732
ClinVar Variation:
2232160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079527.1:p.Ala922Thr
CA187711113
NM_025251.3:c.2764G>A