Canonical Allele Identifier: PA2741951002
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2652255
ClinVar RCV Id: RCV003431286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ser1209Asn
CA408563453
NM_015338.6:c.3626G>A