Canonical Allele Identifier: PA2826873972
Gene: METTL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 218546
ClinVar RCV Id: RCV000203093 RCV004020495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289632.1:p.Ser136Gly
CA249295
NM_001302703.2:c.406A>G