Canonical Allele Identifier: PA156995
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133580
ClinVar RCV Id: RCV000120093 RCV000892843 RCV002259640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Met1249Val
CA156993
NM_015338.6:c.3745A>G