Canonical Allele Identifier: PA2580508958
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804899
ClinVar RCV Id: RCV002471317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733777.1:p.Asn329Ser
CA391926971
NM_170677.5:c.986A>G