Canonical Allele Identifier: PA2828319277
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066241
ClinVar RCV Id: RCV003991245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Cys1161Ser
CA346073532
NM_001369347.1:c.3482G>C
CA346073536
NM_001369347.1:c.3481T>A