Canonical Allele Identifier: PA2828318993
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066241
ClinVar RCV Id: RCV003991245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Cys1363Ser
CA346073532
NM_001369346.1:c.4088G>C
CA346073536
NM_001369346.1:c.4087T>A