Canonical Allele Identifier: PA2828319216
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384509
ClinVar RCV Id: RCV001924849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Met1013Ile
CA346075842
NM_001369347.1:c.3039G>T
CA346075845
NM_001369347.1:c.3039G>C
CA346075847
NM_001369347.1:c.3039G>A