Canonical Allele Identifier: PA2580393774
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099892
ClinVar RCV Id: RCV003021945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Val1069Leu
CA408562571
NM_015338.6:c.3205G>T
CA408562572
NM_015338.6:c.3205G>C