Canonical Allele Identifier: PA2573273965
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480969
ClinVar RCV Id: RCV001994075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Asp1338Asn
CA346074613
NM_018263.6:c.4012G>A