Canonical Allele Identifier: PA2826295376
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804899
ClinVar RCV Id: RCV002471317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001207411.1:p.Asn329Ser
CA391926971
NM_001220482.2:c.986A>G