Canonical Allele Identifier: PA2826291642
Gene: METTL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 435859
ClinVar RCV Id: RCV000504220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193912.1:p.Leu91Val
CA8790111
NM_001206983.2:c.271C>G