Canonical Allele Identifier: PA2828100872
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Gly25Arg
CA3565098
NM_001363626.2:c.73G>C