Canonical Allele Identifier: PA2830351059
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709727
ClinVar RCV Id: RCV002290069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758527.1:p.Arg245Ser
CA391926941
NM_172316.3:c.735A>T
CA391926942
NM_172316.3:c.735A>C