Canonical Allele Identifier: PA915980010
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_004665.2:p.Ile576Val
CA16609517
NM_004674.5:c.1726A>G