Canonical Allele Identifier: PA913198765
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 634618
ClinVar RCV Id: RCV000785146 RCV003279059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Met1373Thr
CA1557358
NM_018263.6:c.4118T>C