Canonical Allele Identifier: PA2828319225
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2878519
ClinVar RCV Id: RCV003707710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Pro1037Leu
CA346075414
NM_001369347.1:c.3110C>T