Canonical Allele Identifier: PA2499284711
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1032033
ClinVar RCV Id: RCV001334011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Leu1311Arg
CA1557396
NM_018263.6:c.3932T>G