ClinGen Allele Registry
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Canonical Allele Identifier:
PA2580471362
Gene: ARHGAP39
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_079527.1:p.Ala922Thr
CA187711113
NM_025251.3:c.2764G>A