Canonical Allele Identifier: PA2830323009
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709727
ClinVar RCV Id: RCV002290069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733775.1:p.Arg333Ser
CA391926941
NM_170675.5:c.999A>T
CA391926942
NM_170675.5:c.999A>C