Canonical Allele Identifier: PA2830350996
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709727
ClinVar RCV Id: RCV002290069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758526.1:p.Arg320Ser
CA391926941
NM_172315.3:c.960A>T
CA391926942
NM_172315.3:c.960A>C