Canonical Allele Identifier: PA2826291737
Gene: METTL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 435859
ClinVar RCV Id: RCV000504220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193916.1:p.Leu24Val
CA8790111
NM_001206987.2:c.70C>G