Canonical Allele Identifier: PA2828108006
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718766
ClinVar RCV Id: RCV002301674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Met1188Leu
CA408563713
NM_001363734.1:c.3562A>C
CA408563714
NM_001363734.1:c.3562A>T