Canonical Allele Identifier: PA2829904967
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_060733.4:p.Cys1421Ser
CA346073532
NM_018263.6:c.4262G>C
CA346073536
NM_018263.6:c.4261T>A