Canonical Allele Identifier: PA2741951013
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2794032
ClinVar RCV Id: RCV003672592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Asn1296Lys
CA9808920
NM_015338.6:c.3888T>A
CA408564007
NM_015338.6:c.3888T>G