ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826291669
Gene: METTL23
HGNC
NCBI
Linked Data
ClinVar Variation Id:
520855
ClinVar RCV Id:
RCV000624880
RCV002060687
RCV003222062
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001193913.1:p.Pro93del
CA8790112
NM_001206984.2:c.278_280del