Canonical Allele Identifier: PA2828319217
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2231804
ClinVar RCV Id: RCV002708262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Val1017Leu
CA346075774
NM_001369347.1:c.3049G>T
CA346075777
NM_001369347.1:c.3049G>C