Canonical Allele Identifier: PA2828100882
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392659
ClinVar RCV Id: RCV001912364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Ala51Val
CA362229228
NM_001363626.2:c.152C>T