Canonical Allele Identifier: PA2573263482
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1537526
ClinVar RCV Id: RCV002166990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Thr1372Ser
CA9808967
NM_015338.6:c.4115C>G
CA408564475
NM_015338.6:c.4114A>T