Canonical Allele Identifier: PA645430443
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_001098684.1:p.Ile482Val
CA16609517
NM_001105214.2:c.1444A>G