Canonical Allele Identifier: PA2828319242
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480969
ClinVar RCV Id: RCV001994075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Asp1078Asn
CA346074613
NM_001369347.1:c.3232G>A