Canonical Allele Identifier: PA645469522
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733777.1:p.Arg333del
CA10576003
NM_170677.5:c.998_1000del
CA391926946
NM_170677.5:c.997A>T
CA391926953
NM_170677.5:c.994A>T
CA391926960
NM_170677.5:c.991A>T