Canonical Allele Identifier: PA2828318979
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3063746
ClinVar RCV Id: RCV003988334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Glu1332Asp
CA1557344
NM_001369346.1:c.3996G>C
CA346073745
NM_001369346.1:c.3996G>T