ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826930211
Gene: ARHGAP39
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001295137.1:p.Ala891Thr
CA187711113
NM_001308208.2:c.2671G>A