Canonical Allele Identifier: PA2826640698
Gene: ASH2L HGNC NCBI

Linked Data

ClinVar Variation Id: 402148
ClinVar RCV Id: RCV000454265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269201.1:p.Ile437Val
CA16609517
NM_001282272.1:c.1309A>G