Canonical Allele Identifier: PA916019342
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_001289632.1:p.Leu91Val
CA8790111
NM_001302703.2:c.271C>G