Canonical Allele Identifier: PA2828318931
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138515
ClinVar RCV Id: RCV003050599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Gln1214His
CA1557419
NM_001369346.1:c.3642G>T
CA346075873
NM_001369346.1:c.3642G>C